BOC-HYP(BZL)-OH
BOC-HYP(BZL)-OH Basic information
- Product Name:
- BOC-HYP(BZL)-OH
- Synonyms:
-
- (4R)-1-Boc-4-(phenylmethoxy)-L-proline
- Boc-Hyp(Bzl)-OH >=98.0% (HPLC)
- BOC-HYP(BZL)-OH·DCHA,98%
- Boc-O-benzyl-L-trans-4-hydroxyproline≥ 98% (HPLC)
- Boc-L-Hyp(Bzl)-OH·DCHA
- Boc-O-benzyl-L-trans-4-hydroxyproline dicyclohexylammonium salt99%
- T-BUTYLOXYCARBONYL-O-BENZYL-L-HYDROXYPROLINE
- 4-hydroxypyrrolidine-1,2-dicarboxylic acid O1-tert-butyl ester O2-(phenylmethyl) ester
- CAS:
- 54631-81-1
- MF:
- C17H23NO5
- MW:
- 321.37
- Product Categories:
-
- Hydroxyproline [Hyp]
- Unusual Amino Acids
- Boc-Amino acid series
- Amino Acid Derivatives
- Amino Acids
- Mol File:
- 54631-81-1.mol
BOC-HYP(BZL)-OH Chemical Properties
- Melting point:
- ~70 °C
- Boiling point:
- 461.3±45.0 °C(Predicted)
- Density
- 1.21±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,2-8°C
- solubility
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- form
- Powder
- pka
- 3.75±0.40(Predicted)
- Appearance
- White to off-white Solid
- optical activity
- [α]20/D 40±2°, c = 2% in ethanol
- BRN
- 5296858
- CAS DataBase Reference
- 54631-81-1(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
BOC-HYP(BZL)-OH Usage And Synthesis
Chemical Properties
White to off-white powder
Uses
Boc-Hyp(Bzl)-OH, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.
reaction suitability
reaction type: Boc solid-phase peptide synthesis
Synthesis
136024-60-7
40350-83-2
General procedure for the synthesis of 4-(benzyloxy)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid from 1-(tert-butyl) 2-methyl (2S,4R)-4-(benzyloxy)pyrrolidine-1,2-dicarboxylic acid ester: lithium hydroxide was added to a mixture of THF and H2O (60 mL, 2:1, v/v/v/v/v) of compound 2 (3.45 g, 10.29 mmol) monohydrate (1.29 g, 30.87 mmol). The reaction mixture was stirred at room temperature for 3 hours. After the completion of the reaction was monitored by TLC, the reaction mixture was concentrated under reduced pressure, acidified to pH < 7 with 1N hydrochloric acid solution and subsequently extracted with ethyl acetate (3 x 30 mL). The organic layers were combined, washed with saturated sodium chloride solution (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by grinding with pentane (20 mL) to give compound 3 (3.21 g, 97% yield) in white solid form. Mass spectrum (ESI) m/z 322 [M+H]+.
References
[1] Patent: US9994614, 2018, B2. Location in patent: Page/Page column 51; 52; 53
[2] Patent: WO2012/146666, 2012, A1. Location in patent: Page/Page column 206
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BOC-HYP(BZL)-OH(54631-81-1)Related Product Information
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