Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722003Generated: October 26, 2026

2-Bromo-1-(thiophen-2-yl)ethan-1-one → HCID 178488931, compound

https://huagongshe.com/reaction/1722003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(thiophen-2-yl)ethan-1-oneHCID 2776372—
ReactantHCID 13621616HCID 13621616—
SolventChloroformHCID 6212—
ProductHCID 178488931HCID 17848893179.3%

Reaction Steps

A slurry of 22 (21.6 g, 0.132 mol) in CHCl2 (300 ml) was treated dropwise over 15 minutes with 2-(bromoacetyl)-thiophene (10.84, 0.0476 mol, 92% pure) in CHCl3 (55 ml). The reaction mixture was stirred at room temperature for 24 hours, and then filtered to remove 10.2 g of the hydrobromide of 22. The mother liquors were concentrated to a semisolid which was swirled with 75 ml of methylene chloride and refrigerated overnight. The resultant gray solid was washed with CH2Cl2 and dried to give 10.2 grams (79%) of 23; m.p. 110°-114°. The analytical sample was dried in vacuo at 85°, m.p. 115°-117°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853383
Source datasetuspto-grants-1989_08
ORD IDord-ee5302d83aa5462dbfd955771fa16922
Source noteuspto-grants-1989_08