(R)-1-N-Boc-beta-proline
- Product Name
- (R)-1-N-Boc-beta-proline
- CAS No.
- 72925-16-7
- Chemical Name
- (R)-1-N-Boc-beta-proline
- Synonyms
- B67255;BOC-L-B-PROLINE;Boc-D-beta-Proline;(3S)-BOC-BETA-PRO-OH;N-Boc-D-beta-proline;(R)-N-Boc-Beta-Proline;N-Boc-D-^b-proline, 95%;(R)-1-N-Boc-beta-proline;(S)-1-N-BOC-BETA-PROLINE;R-Boc-Pyrrolidine-3-carboxylic
- CBNumber
- CB7225932
- Molecular Formula
- C10H17NO4
- Formula Weight
- 215.25
- MOL File
- 72925-16-7.mol
(R)-1-N-Boc-beta-proline Property
- Melting point:
- 138-143°C
- Boiling point:
- 337.2±35.0 °C(Predicted)
- Density
- 1.201±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- Soluble in Dimethyl sulfoxide (DMSO).
- form
- solid
- pka
- 4.47±0.20(Predicted)
- color
- White to off-white
- optical activity
- [α]/D -15.0, c = 0.5% in chloroform
- InChI
- InChI=1S/C10H17NO4/c1-10(2,3)15-9(14)11-5-4-7(6-11)8(12)13/h7H,4-6H2,1-3H3,(H,12,13)/t7-/m1/s1
- InChIKey
- HRMRQBJUFWFQLX-SSDOTTSWSA-N
- SMILES
- N1(C(OC(C)(C)C)=O)CC[C@@H](C(O)=O)C1
- CAS DataBase Reference
- 72925-16-7(CAS DataBase Reference)
Safety
- Hazard Codes
- N
- Risk Statements
- 36/37/38-50
- Safety Statements
- 26-36/37/39-61
- RIDADR
- UN 3077 9 / PGIII
- WGK Germany
- 3
- HS Code
- 29339900
N-Bromosuccinimide Price
- Product number
- 735493
- Product name
- (R)-1-Boc-3-pyrrolidinecarboxylic acid
- Purity
- 97%
- Packaging
- 500mg
- Price
- $113.97
- Updated
- 2025/07/31
- Product number
- B809535
- Product name
- (R)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxylicAcid
- Packaging
- 500mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- S922
- Product name
- (R)-1-Boc-3-carboxylpyrrolidine
- Packaging
- 250mg
- Price
- $26
- Updated
- 2021/12/16
- Product number
- CS-B0422
- Product name
- (R)-1-N-Boc-beta-proline
- Purity
- ≥97.0%
- Packaging
- 1g
- Price
- $38
- Updated
- 2021/12/16
- Product number
- J93496
- Product name
- (R)-1-Boc-3-carboxylpyrrolidine
- Packaging
- 1g
- Price
- $49
- Updated
- 2021/12/16
(R)-1-N-Boc-beta-proline Chemical Properties,Usage,Production
Uses
It is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuffs.
Synthesis
122684-33-7
72925-16-7
General procedure for the synthesis of (R)-1-Boc-3-carboxypyrrolidine from methyl 1-Boc-pyrrolidine-3-carboxylate: sodium hydroxide (0.80 g, 20.00 mmol) was dissolved in water (15 mL), and this solution was added to a methanol (30 mL) solution of methyl 1-Boc-pyrrolidine-3-carboxylate (2.30 g, 10.00 mmol). . The reaction mixture was allowed to react for 3 hours with stirring at room temperature. After the reaction was completed, the methanol was removed by concentration under reduced pressure. The pH of the remaining solution was adjusted to 4 with 2 M glacial acetic acid and then extracted with dichloromethane (50 mL x 3). The organic phases were combined and dried with anhydrous sodium sulfate. After filtration, the organic phase was concentrated under reduced pressure to give 1.80 g of an oily product in 83.00% yield.
References
[1] Organic Letters, 2005, vol. 7, # 15, p. 3287 - 3289
[2] Journal of Medicinal Chemistry, 2001, vol. 44, # 1, p. 94 - 104
[3] European Journal of Organic Chemistry, 2005, # 4, p. 673 - 682
[4] Patent: CN106336413, 2017, A. Location in patent: Paragraph 0453; 0454; 0455
[5] Journal of Medicinal Chemistry, 1990, vol. 33, # 7, p. 2052 - 2059
(R)-1-N-Boc-beta-proline Preparation Products And Raw materials
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