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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848112Generated: October 31, 2026

Chlorosuccinimide → 2-Chloro-3-(2-(methylthio)benzo[d]thiazol-6-yl)propanal

https://huagongshe.com/reaction/1848112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantL-ProlineHCID 145742—
Reactant3-(2-(Methylthio)benzo[d]thiazol-6-yl)propanalHCID 86681086—
SolventDichloromethaneHCID 6344—
Product2-Chloro-3-(2-(methylthio)benzo[d]thiazol-6-yl)propanalHCID 8668108779.7%

Reaction Steps

L-proline (0.22 g, 1.9 mmol) was added to a solution of 3-(2-(methylthio)benzo[d]thiazol-6-yl)propanal (2.3 g, 9.7 mmol) in DCM (40 mL) at 0° C. followed by addition of N-chlorosuccinimide (1.4 g, 10 mmol). The reaction mixture was slowly warmed to ambient temperature and stirred overnight. The reaction mixture was concentrated under reduced pressure and purified by silica gel chromatography, eluting with 10:1 to 2:1 petroleum ether/EtOAc to afford 2-chloro-3-(2-(methylthio)benzo[d]thiazol-6-yl)propanal as a yellow oil (2.1 g, 79%). 1H NMR (300 MHz, CDCl3) δ 9.56 (dd, J=1.2, 2.1 Hz, 1H), 7.81 (d, J=8.4 Hz, 1H), 7.63 (d, J=0.6 Hz, 1H), 7.28 (d, J=1.5 Hz, 1H), 4.44-4.39 (m, 1H), 3.51-3.44 (m, 1H), 3.20-3.13 (m, 1H), 2.78 (s, 3H). LCMS (ESI) m/z 290 (M+18+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-8f0bab065beb491aa91474afc309d9e2
Source noteuspto-grants-2015_02