1-Boc-4-(2-hydroxyethyl)piperidine
- Product Name
- 1-Boc-4-(2-hydroxyethyl)piperidine
- CAS No.
- 89151-44-0
- Chemical Name
- 1-Boc-4-(2-hydroxyethyl)piperidine
- Synonyms
- tert-butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate;Tirofiban Impurity 57;N-BOC-4-PIPERIDINEETHANOL;1-Boc-4-piperidineethanol;1-BOC-4-PIPERIDINE EHTANOL;BOC-2-(4-PIPERIDYL)ETHANOL;1-Boc-4-(hydroxyethyl)pip...;N-BOC-4-piperidine-β-ethanol;N-Boc-4-piperidineethanol 97%;N-Boc-4-piperidineethanol 97%
- CBNumber
- CB9449817
- Molecular Formula
- C12H23NO3
- Formula Weight
- 229.32
- MOL File
- 89151-44-0.mol
1-Boc-4-(2-hydroxyethyl)piperidine Property
- Boiling point:
- 120-150 °C/0.5 mmHg (lit.)
- Density
- 1.043 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.4730(lit.)
- Flash point:
- >230 °F
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- viscous liquid
- pka
- 15.10±0.10(Predicted)
- color
- Colourless to light yellow
- InChI
- InChI=1S/C12H23NO3/c1-12(2,3)16-11(15)13-7-4-10(5-8-13)6-9-14/h10,14H,4-9H2,1-3H3
- InChIKey
- YBNJZIDYXCGAPX-UHFFFAOYSA-N
- SMILES
- N1(C(OC(C)(C)C)=O)CCC(CCO)CC1
- CAS DataBase Reference
- 89151-44-0(CAS DataBase Reference)
Safety
- Hazard Codes
- Xi
- WGK Germany
- 3
- HS Code
- 2933399990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P337+P313IF eye irritation persists: Get medical advice/attention.
N-Bromosuccinimide Price
- Product number
- 547247
- Product name
- N-Boc-4-piperidineethanol
- Purity
- 97%
- Packaging
- 5g
- Price
- $58.58
- Updated
- 2025/07/31
- Product number
- 547247
- Product name
- N-Boc-4-piperidineethanol
- Purity
- 97%
- Packaging
- 1g
- Price
- $30
- Updated
- 2023/06/20
- Product number
- B657230
- Product name
- N-BOC-4-piperidine-β-ethanol
- Packaging
- 10g
- Price
- $200
- Updated
- 2021/12/16
- Product number
- 4H01-1-X3
- Product name
- 4-(2-Hydroxyethyl)piperidine, N-Boc protected
- Packaging
- 25g
- Price
- $136
- Updated
- 2021/12/16
- Product number
- 069039
- Product name
- tert-Butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate
- Purity
- >95%
- Packaging
- 25g
- Price
- $145
- Updated
- 2021/12/16
1-Boc-4-(2-hydroxyethyl)piperidine Chemical Properties,Usage,Production
Uses
N-BOC-4-piperidine-β-ethanol is used to prepare anilinoquinazoline VEGF receptor tyrosine kinase inhibitors with antitumor activities. It is also used to synthesize 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists with antiviral activities.
Synthesis
135716-08-4
89151-44-0
General procedure for the synthesis of N-Boc-4-piperidine ethanol from tert-butyl 4-(2-ethoxy-2-oxo-substituted)piperidine-1-carboxylate: first, the above product (639 mg, 2.4 mmol) was dissolved in 6 mL of methanol, protected by argon, replaced three times with hydrogen and reacted overnight in a hydrogenation unit (4 atm H2). Upon completion of the reaction, the reaction solution was filtered through diatomaceous earth and washed with ethyl acetate. The filtrate was concentrated and purified by column chromatography to give a white solid product (722 mg, 100% yield). Subsequently, the above product (506 mg, 1.9 mmol) was dissolved in 10 mL of ether, cooled to -20 °C, and hydrogenated diisobutylaluminum (1.0 M, 5 mL, 5 mmol) was slowly added, and the reaction was carried out for 10 min until the raw material completely disappeared. The reaction mixture was poured into saturated potassium sodium tartrate solution and stirred at room temperature for 3 hours until clarified. The aqueous phase was extracted three times with ether, the organic phases were combined, washed with saturated NaCl solution and dried over anhydrous Na2SO4. After concentration, the product was purified by column chromatography to give a white solid product (368 mg, 86% yield).
References
[1] Patent: CN102952072, 2016, B. Location in patent: Paragraph 0110-0111
[2] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 13, p. 2167 - 2172
[3] Patent: US2012/71461, 2012, A1
[4] Patent: CN107793408, 2018, A
[5] Patent: WO2018/68297, 2018, A1
1-Boc-4-(2-hydroxyethyl)piperidine Preparation Products And Raw materials
Raw materials
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View Lastest Price from 1-Boc-4-(2-hydroxyethyl)piperidine manufacturers
- Product
- 1-Boc-4-(2-hydroxyethyl)piperidine 89151-44-0
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 1ton
- Release date
- 2018-08-06
- Product
- 1-Boc-4-(2-hydroxyethyl)piperidine 89151-44-0
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 1000KG
- Release date
- 2018-08-09