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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153956Generated: October 27, 2026

3-Chloro-2-methylaniline → 2-(3-Chloro-2-methylphenyl)thiophene

https://huagongshe.com/reaction/1153956

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methylanilineHCID 6894—
ReactantThiopheneHCID 8030—
ReactantTert-Butyl nitriteHCID 10906—
Product2-(3-Chloro-2-methylphenyl)thiopheneHCID 13243416—

Reaction Steps

3-Chloro-2-methylaniline was treated with t-butylnitrite in excess thiophene as described in J. Chem. Soc., 4257 (1963) to produce 2-(3-chloro-2-methylphenyl)thiophene as an oil. Reaction of the oil with N-bromosuccinimide as described in J. Am. Chem. Soc., 89, 2348 (1967) yielded 2-(2-bromomethyl-3-chlorophenyl)thiophene as an oil, which was reacted without further purification, as described in J. Chem. Soc., 2708 (1955), with diethyl malonate in the presence of tetrabutyl ammonium bromide and potassium hydroxide in dry tetrahydrofuran, producing ethyl [2-carboethoxy-3-[2-chloro-6-(thien-2-yl)phenyl]]propionate. Hydrolysis of the latter with hydrochloric acid in glacial acetic acid provided 3-[2-chloro-6-(thien-2-yl)phenyl]propionic acid; mp 83°-86°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487778
Source datasetuspto-grants-1984_12
ORD IDord-6dd2cef81a444b8a86f8eb351140693e
Source noteuspto-grants-1984_12