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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651836Generated: October 26, 2026

Acetyl chloride → Z-Hse(Ac)-OH

https://huagongshe.com/reaction/651836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantCbz-L-HomoserineHCID 489187—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
ProductZ-Hse(Ac)-OHHCID 1183332367.1%

Reaction Steps

1.27 g (5 mmol) of N-benzyloxycarbonyl-L-homoserine are dissolved in 5 ml of acetic acid, and 0.41 g (5 mmol) of sodium acetate is added. 1.19 g (15 mmol) of acetyl chloride are then added and stirring is carried out for one hour. The acetic acid and the excess acetyl chloride are removed in vacuo, the residue is taken up in 30 ml of methyl isobutyl ketone and 30 ml of water, and the pH is adjusted to 8 using 50% sodium hydroxide solution. The aqueous phase is separated off, adjusted to pH=2 using hydrochloric acid and extracted using 30 ml of methyl isobutyl ketone. Concentration of the organic phase in vacuo yields 0.99 g (67%) of N-benzyloxycarbonyl—O—acetyl-L-homoserine in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281364B1
Source datasetuspto-grants-2001_08
ORD IDord-436e184255444bcf8e6098e637b9f9bb
Source noteuspto-grants-2001_08