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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739064Generated: November 2, 2026

Acetyl chloride → HCID 18696167, compound

https://huagongshe.com/reaction/1739064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 18696107HCID 18696107—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18696167HCID 18696167109%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 3-(2-(N-t-butoxycarbonylamino)ethoxy)-5-hydroxy-1,2-benzisoxazole (100 mg) in tetrahydrofuran (5 ml) was added triethylamine (44 mg) and acetyl chloride (34 mg) with stirring at 5° C., and the mixture was then stirred at the same temperature for 15 minutes. The reaction mixture was poured into ice water (40 ml), extracted with ethyl acetate (twice each with 40 ml) and the combined extracts were dried over anhydrous magnesium sulphate and filtered. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography with cyclohexane/ethyl acetate (9/1) as an eluent, to give the title compound (101 mg, 88%) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965591
Source datasetuspto-grants-1999_10
ORD IDord-e3f1074d18e14354a598cb646b748b31
Source noteuspto-grants-1999_10