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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419113Generated: October 29, 2026

Acetyl chloride → HCID 22119058, compound

https://huagongshe.com/reaction/1419113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 22119052HCID 22119052—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22119058HCID 22119058—

Reaction Steps

5.64 ml of dehydrated triethylamine and 2.9 ml of acetyl chloride were added at room temperature to a solution of 7.2 g of N-t-butoxycarbonyl-N-methyl-4-hydroxy-2,3,5-trimethylaniline (prepared as described in Preparation 15) in 100 ml of dehydrated tetrahydrofuran, and the resulting mixture was stirred for 1 hour, after which it was allowed to stand overnight. The reaction mixture was then diluted with water and the aqueous mixture was extracted with ethyl acetate. The extract was washed with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, after which the residue was triturated with ice-cooled hexane to cause crystallization. The crystals were collected by filtration and washed with ice-cooled hexane to give 6.25 g of the title compound, melting at 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886014
Source datasetuspto-grants-1999_03
ORD IDord-60cb366da1304f7d95ee82a36f0765f2
Source noteuspto-grants-1999_03