HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407948Generated: October 30, 2026
Sodium Hydroxide → (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((R)-2,3-dihydroxypropylthio)propanoate
https://huagongshe.com/reaction/2407948
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Nitrobenzoate | HCID 5159892 | — |
| Reactant | tert-butyl (2R)-2-{[(benzyloxy)carbonyl]amino}-3-sulfanylpropanoate | HCID 86678278 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((R)-2,3-dihydroxypropylthio)propanoate | HCID 67400883 | — |
Reaction Steps
A solution of (25)-(+)-glycidyl-4-nitrobenzoate (1.1 eq) and 1M NaOH (1.1 eq) in tBuOH (0.1 M) was stirred at room temperature until complete hydrolysis of the nitrobenzoate was observed (30 minutes). To the resulting mixture, a solution of (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-mercaptopropanoate (12, 1 eq) in tBuOH (1 M) was introduced and the reaction stirred at room temperature for 15 hours. The reaction mixture was concentrated en vaccuo to remove tBuOH then dissolved in EtOAc. The EtOAc solution was washed three times with water, once with brine, then dried over Na2SO4 and concentrated. The crude material was purified by flash chromatography on a COMBIFLASH® system (ISCO) using a gradient of 0-90% EtOAc/Hex to give the title product as a colorless viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08808703B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-4d62bb6e612445af843f7746baf89690 |
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| Source note | uspto-grants-2014_08 |
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