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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386930Generated: October 31, 2026

Acetyl chloride → HCID 86757198, compound

https://huagongshe.com/reaction/1386930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 21180500HCID 21180500—
ReactantEthanol hydrochlorideHCID 21887872—
SolventDichloromethaneHCID 6344—
ProductHCID 86757198HCID 8675719896%

Reaction Steps

A solution of (RS)-1-{3-[5-(4-methoxy-phenyl)-1H-[1,2,4]triazol-3-yl]-benzyl}-pyrrolidin-3-ol hydrochloride (1:1) (mixture of tautomers) (50 mg, 0.13 mmol) in CH2Cl2 (5 ml) was treated with triethylamine (26 mg, 0.26 mmol 2 eq.) and stirred for 30 min. at r.t. Acetyl chloride (11 mg, 0.13 mmol, 1 eq.) was added and stirring was continued for 1.5 hrs. After removal of the solvent the residue was chromatographed over 20 g SiO2 (Merck 230-400 mesh) with CH2Cl2-MeOH (2M NH3) 96:4. The resulting product was dissolved in ethanol at r.t. and an excess 1.45 N HCl/EtOH solution (0.1 ml, 0.14 mmol) was added. After 30 min. stirring the solvent was evaporated and the residue dried under high vacuum at 40° C. overnight affording the title compound (53 mg, 0.12 mmol, 96% yield) as a colorless solid. MS: m/e=393.2 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265426B1
Source datasetuspto-grants-2001_07
ORD IDord-ffcc3675e90a4f30916fd7a58c48874f
Source noteuspto-grants-2001_07