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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298634Generated: November 2, 2026

Phenacyl bromide → HCID 18537476, compound

https://huagongshe.com/reaction/2298634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantHCID 18537366HCID 18537366—
ProductHCID 18537476HCID 18537476—

Reaction Steps

A solution of 375 mg (1.54 mmol) of isopropyl 4-(aminothioxomethyl)-5-methylthiophene-2-carboxylate was reacted with 307 mg (1.54 mmol) of 2-bromoacetophenone (Aldrich, Milwaukee, Wis., USA) in a manner similar to Example 8, step (a) to give, after crystallization from methanol, isopropyl 5-methyl-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxylate (347 mg, 66%) as light brown needles. 1H-NMR (DMSO-d6; 300 MHz) δ8.23 (s, 1H), 8.09 (s, 1H), 8.05 (m, 2H), 7.49 (m, 2H), 7.38 (m, 1H), 5.13 (septet, 1H, J=6.2 Hz), 2.86 (s, 3H), 1.33 (d, 6H, J=6.2 Hz). Mass spectrum (ESI, m/z): Calcd. for C18H17NO2S2 344.1 (M+H), found 344.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-d88f199dbb314c1e9028121afa302216
Source noteuspto-grants-2002_12