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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699971Generated: November 3, 2026

Ethylbenzene → (2S,3S)-1-Acetoxy-3-(t-butoxycarbonylamino)-2-hydroxy-4-phenylbutane

https://huagongshe.com/reaction/1699971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylbenzeneHCID 7500—
ReactantPotassium AcetateHCID 517044—
Reactant1,1-Dimethylethyl N-((1S,2S)-3-chloro-2-hydroxy-1-(phenylmethyl)propyl)carbamateHCID 7146645—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
Product(2S,3S)-1-Acetoxy-3-(t-butoxycarbonylamino)-2-hydroxy-4-phenylbutaneHCID 1105639845%

Reaction Steps

A mixture composed of 2.0 mmol (0.599 g) of (2S, 3S)-3-(t-butoxycarbonylamino)-1-chloro-2-hydroxy-4-phenylbutane, 0.1 mmol (0.032g) of tetrabutylammoniumbromide, 5.0mmol (0.49 g) of potassium acetate and 10 ml of acetonitrile was stirred under reflux for 50 hours. Thereafter, the solvent was distilled off under reduced pressure, 20 ml of water and 20 ml of ethyl acetate were added, and the organic layer was separated, dried over sodium sulfate, filtered and concentrated under reduced pressure to give a crude product. Quantitative analysis was curried out by high performance liquid chromatography using ethylbenzene as an internal standard. Thus was obtained 0.289 g (45%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348615B2
Source datasetuspto-grants-2002_02
ORD IDord-7d3e368f049f4b90bb383430c1b0281a
Source noteuspto-grants-2002_02