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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482528Generated: October 30, 2026

Acetyl chloride → HCID 22119058, compound

https://huagongshe.com/reaction/482528

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 step (f) above] 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 numberUS05798375
Source datasetuspto-grants-1998_08
ORD IDord-f3b20e4d9e51414890ac05daed3fc7da
Source noteuspto-grants-1998_08