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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197440Generated: October 31, 2026

Chloroacetyl chloride → HCID 52952411, compound

https://huagongshe.com/reaction/2197440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
ReactantHCID 86654171HCID 86654171—
SolventDichloromethaneHCID 6344—
ProductHCID 52952411HCID 5295241195%

Reaction Conditions

Temperature-15 °C

Reaction Steps

168 mg (1 eq.) of 4-(3-thiophen-2-yl[1,2,4]oxadiazol-5-yl)-piperidinium hydrochloride obtained in step 1) above and 220 μl (3.1 eq.) of triethylamine were dissolved in 1 ml of dichloromethane and stirred at a temperature of −15° C. A solution of chloroacetyl chloride (40 μl, 1 eq.) in 1 ml of dichloromethane (CH2Cl2) was added dropwise to the resulting suspension. The resulting mixture was stirred at room temperature for 2 hours. 20 ml of dichloromethane were then added, and the resulting organic phase was washed with three times 50 ml of 5% hydrochloric acid and then dried over MgSO4, filtered and evaporated. 2-Chloro-1-[4-(3-thiophen-2-yl[1,2,4]oxa-diazol-5-yl)piperid-1-yl]ethanone was obtained in the form of a white solid, in a yield of 95%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338599B2
Source datasetuspto-grants-2012_12
ORD IDord-a1a484ab68cf4ab5858b809a13d501fb
Source noteuspto-grants-2012_12