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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066290Generated: November 1, 2026

Acetyl chloride → HCID 54557979, compound

https://huagongshe.com/reaction/1066290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 54557979HCID 5455797970%

Reaction Steps

N-(tert-Butoxycarbonyl)-L-alaninol (438 mg, 2.5 mmol) was dissolved in 5 mL of methylene chloride in an ice bath and acetyl chloride (0.294 mL, 3.75 mmol), followed by triethylamine (0.7 mL, 5 mmol) were added. It was then reacted at 0° C. for 1 hour and at room temperature for 2 days. The mixture was diluted with 25 mL of ethyl acetate and the organic layer was washed with 10%-sodium hydrogen carbonate (3x), brine (2x), dried over magnesium sulfate anhydrous, and then evaporated to dryness to yield 380 mg of N-(tert-butoxycarbonyl)-O-acetyl-L-alaninol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242494B1
Source datasetuspto-grants-2001_06
ORD IDord-ae264358f1344d778eb797c8c4d1b6d2
Source noteuspto-grants-2001_06