(R)-1-N-Boc-beta-proline
(R)-1-N-Boc-beta-proline Basic information
- Product Name:
- (R)-1-N-Boc-beta-proline
- Synonyms:
-
- (S)-1-N-BOC-BETA-PROLINE
- S-1-BOC-PYRROLIDINE-3-CARBOXYLIC ACID
- (S)-PYRROLIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER
- BOC-L-B-PROLINE
- BOC-(3S)-1-PYRROLIDINE-3-CARBOXYLIC ACID
- (3S)-BOC-1-PYRROLIDINE-3-CARBOXYLIC ACID
- (3S)-BOC-BETA-PRO-OH
- (3R)-1-(tertbutoxycarbonyl)pyrrolidine-3-carboxylic acid
- CAS:
- 72925-16-7
- MF:
- C10H17NO4
- MW:
- 215.25
- EINECS:
- 674-617-4
- Product Categories:
-
- pharmacetical
- Pyrrole&Pyrrolidine&Pyrroline
- Mol File:
- 72925-16-7.mol
(R)-1-N-Boc-beta-proline Chemical Properties
- 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 Information
- 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
(R)-1-N-Boc-beta-proline Usage And Synthesis
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-prolineSupplier
- Tel
- 0512-68323967 18015559028
- sales@iticmedchem.com
- Tel
- 0513-82104991 18912868361
- sales11@btcpharm.com
- Tel
- 13501719342; 13501719342
- wayne.zheng@elucigenbio.com
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- +86-21-20908456
- sales@BioChemBest.com
(R)-1-N-Boc-beta-proline(72925-16-7)Related Product Information
- (S)-1-N-BOC-BETA-PROLINE
- 1-(tert-Butoxycarbonyl)-3-pyrrolidinol
- (R)-1-Boc-3-Hydroxypiperidine
- BOC-1,3-CIS-ACHC-OH
- CYCLOHEXANECARBOXYLIC ACID, 3-[[(1,1-DIMETHYLETHOXY)CARBONYL]AMINO]-, (1R,3S)-
- (1R,2S,3R,4R)-2,3-DIHYDROXY-4-(HYDROXYMETHYL)-1-AMINOCYCLOPENTANE HYDROCHLORIDE
- (R)-1-N-BOC-BETA-PROLINE
- 1-Boc-Pyrrolidine
- (R)-1-Boc-pyrrolidine-3-carboxylic acid methyl ester
- (S)-1-Boc-pyrrolidine-3-carboxylic acid methyl ester
- R/S-1-N-BOC-BETA-PROLINE
- 1-N-BOC-BETA-PROLINE