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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583508Generated: November 1, 2026

Acetyl chloride → HCID 13336145, compound

https://huagongshe.com/reaction/1583508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 9835457HCID 9835457—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13336145HCID 1333614570%

Reaction Steps

To the stirred solution of 3-(benzyloxycarbonylamino)-N-(2-mercaptoethyl)propionamide (2 g) and triethylamine (0.8 g) in anhydrous THF (15 ml), acetyl chloride (0.6 g) is added dropwise under ice-water cooling. After the addition, the mixture is stirred for 30 minutes under ice-water cooling and additional 30 minutes at room temperature. The solution is filtered and the filtrate is concentrated in vacuo. The residue is dissolved in ethyl acetate (30 ml) and the solution is washed with saturated sodium bicarbonate solution, N hydrochloric acid and then saturated sodium chloride solution. The ethyl acetate solution is dried over anhydrous magnesium sulfate and concentrated in vacuo to give 1.6 g (70%) of the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552765
Source datasetuspto-grants-1985_11
ORD IDord-88bbf8ec53c64411a17556a8a8210b23
Source noteuspto-grants-1985_11