HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843283Generated: October 31, 2026
Hydrochloric Acid → (2R,3S)-3-(t-butoxycarbonyl)amino-4-phenyl-butane-1,2-diol
https://huagongshe.com/reaction/843283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl ester | HCID 11449720 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2R,3S)-3-(t-butoxycarbonyl)amino-4-phenyl-butane-1,2-diol | HCID 11076870 | — |
Reaction Steps
A solution of N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenylbutyric acid methyl ester 154.7 g dissolved in ethanol 300 ml was kept at 5-15° C. and mixed with sodium borohydride 24.6 g and stirred at 15-45° C. for 3hrs. The reaction solution was cooled and adjusted with 3N-HCl to pH 2.5-3.5. Water was added to the resultant solution and then the obtained solution was cooled to 5° C. or lower to deposit crystals. The crystals were filtered, dissolved in ethyl acetate, and washed with aqueous 5% sodium bicarbonate solution to separate an organic phase, which was washed with aqueous 10% sodium chloride solution and concentrated under an reduced pressure to obtain the crude N-tert-butoxycarbonyl-3(S)-amino-2(R)-hydroxy-4-phenyl-1-butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06376685B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-cc979490d8a7469887043eb97502b186 |
|---|
| Source note | uspto-grants-2002_04 |
|---|