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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192051Generated: November 4, 2026

2,4-Dichlorobenzenethiol → 2-(2,4-Dichlorophenyl)sulfanyl-5-methylsulfonyl-3-nitro-thiophene

https://huagongshe.com/reaction/1192051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzenethiolHCID 70730—
Reactant2-Bromo-5-methanesulfonyl-3-nitrothiopheneHCID 60207310—
Product2-(2,4-Dichlorophenyl)sulfanyl-5-methylsulfonyl-3-nitro-thiopheneHCID 4693214625%

Reaction Steps

Prepared by a similar procedure to that described as in Step D for example 22 from the 2-bromo-5-methylsulfonyl-3-nitro-thiophene (148 mg, 0.52 mmol) and 2,4-dichlorobenzenethiol (100 mg, 0.56 mmol) to afford the title product as a solid (50 mg, 25% yield). 1H NMR (400 MHz, d6-DMSO) δ: 8.35 (1H, s), 8.10 (1H, m), 8.20 (1H, m), 7.74 (1H, m), 3.42 (3H, s). MS m/z: 381.81 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680139B2
Source datasetuspto-grants-2014_03
ORD IDord-63ed1969cba34546b7e47c6814407508
Source noteuspto-grants-2014_03