Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207138Generated: November 1, 2026

Acetyl chloride → HCID 10609791, compound

https://huagongshe.com/reaction/2207138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant(S)-(+)-2-Oxo-4-phenyl-3-oxazolidineacetic acidHCID 853681—
SolventMethanolHCID 887—
ProductHCID 10609791HCID 1060979194%

Reaction Steps

A solution of (4(S)-phenyloxazolidin-2-on-3-yl)acetic acid (1 g, 4.52 mmol) (prepared according to Evans in U.S. Pat. No. 4,665,171) in 20 mL of anhydrous methanol was treated hourly with 5 equivalents of acetyl chloride, for a total of 20 equivalents. The resulting solution was stirred overnight. The residue obtained after evaporation of the MeOH was redissolved in 30 mL of CH2Cl2 and treated with 50 mL of saturated aqueous Na2CO3. The organic layer was evaporated and dried (MgSO4) to yield the title compound as a colorless oil (1.001 g, 94%); 1H NMR (CDCl3) δ 3.37 (d, J==18.0 Hz, 1H), 3.69 (s, 3H), 4.13 (t, J=8.3 Hz, 1H), 4.28 (d, J=18.0 Hz, 1H), 4.69 (t, J=8.8 Hz, 1H), 5.04 (t, J=8.4 Hz, 1H), 7.26-7.29 (m, 2H), 7.36-7.42 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376424B2
Source datasetuspto-grants-2016_06
ORD IDord-0196c2cca5874758a8437e143103bec6
Source noteuspto-grants-2016_06