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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397221Generated: October 30, 2026

Bromomethyl 4-methoxyphenyl ketone → 2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]acetonitrile

https://huagongshe.com/reaction/1397221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
Reactant2-CyanoethanethioamideHCID 1416277—
Product2-[4-(4-methoxyphenyl)-1,3-thiazol-2-yl]acetonitrileHCID 233731075%

Reaction Steps

This compound was synthesized from 2-bromo-1-(4-methoxyphenyl)ethanone and 2-cyanothioacetamide as described in example 1 step 1 (1.5 g, yield 75%). 1H NMR (300 MHz, CDCl3) δ 7.83 (d, J=8.9 Hz, 2H), 7.35 (s, 1H), 6.98 (d, J=8.9 Hz, 2H), 4.17 (s, 2H), 3.86 (s, 3H). MS (ESI) m/z: Calculated for C12H10N2OS: 230.05. found: 231.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901156B2
Source datasetuspto-grants-2014_12
ORD IDord-be9e1db6d0124d6d9a24ccbbd2845a3d
Source noteuspto-grants-2014_12