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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-2-methylaniline | HCID 6894 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Product | 2-(3-Chloro-2-methylphenyl)thiophene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04487778 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-6dd2cef81a444b8a86f8eb351140693e |
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| Source note | uspto-grants-1984_12 |
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