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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397205Generated: October 28, 2026

Hexamethyldisilazane → Rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-acetamide

https://huagongshe.com/reaction/397205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexamethyldisilazaneHCID 13838—
ReactantOxalyl chlorideHCID 65578—
ReactantRac-cyclopentyloxy-(3,4-dichloro-phenyl)-acetic acidHCID 12044174—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductRac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-acetamideHCID 1817259671%

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) solution of rac-cyclopentyloxy-(3,4-dichloro-phenyl)-acetic acid (Example 1; 164 mg, 0.57 mmol) in dichloromethane (10 mL) and N,N-dimethylformamide (one drop) was treated with oxalyl chloride (2.0 M solution in dichloromethane, 0.43 mL, 0.86 mmol). The reaction was stirred at 0° C. for 1 h, then 1,1,1,3,3,3-hexamethyldisilazane (0.42 mL, 2.0 mmol) was added and the resulting cloudy mixture was stirred at 25° C. for 16 h. The reaction was quenched with methanol (10 mL), washed with an aqueous solution of 5% sulfuric acid (2×15 mL) and extracted with dichloromethane (3×10 mL). The combined organic extracts were washed with brine (1×10 mL), then were dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 60/40 hexanes/ethyl acetate) to give rac-2-cyclopentyloxy-2-(3,4-dichloro-phenyl)-acetamide (116 mg, 71% yield) as a white solid, mp 88.3-91.4° C.; FAB-HRMS m/e calcd for C13H15NCl2O2 (M+) 288.0558, found 288.0572.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608218B2
Source datasetuspto-grants-2003_08
ORD IDord-c7825444f52744d4b5ba9faabf7e209b
Source noteuspto-grants-2003_08