HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903470Generated: November 2, 2026
2-Bromoisovaleric acid → 2-[(2,3-Dichloro-4-methoxyphenyl)sulfanyl]-3-methylbutanoic acid
https://huagongshe.com/reaction/1903470
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoisovaleric acid | HCID 11268 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,3-Dichloro-4-methoxybenzene-1-thiol | HCID 15914269 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[(2,3-Dichloro-4-methoxyphenyl)sulfanyl]-3-methylbutanoic acid | HCID 15914270 | 80.5% |
Reaction Steps
To 3.13 g of 99% sodium hydride under nitrogen at room temperature is added a solution of 12.26 g of 2,3-dichloro-4-methoxythiophenol in 100 ml of sieve-dried dimethylformamide over 2 minutes. The reaction is stirred for 12 minutes. A solution of 9.56 g of α-bromoisovaleric acid in 85 ml of dimethylformamide is added over 4 minutes. The reaction is stirred at room temperature for 3 hours, cooled in ice, diluted with 500 ml of water and filtered. The solution is cooled and acidified with 3 N hydrochloric acid to give the product. The precipitate is filtered, washed with a small amount of water, dried and recrystallized from acetone-pentane to give 13.14 g of α-(2,3-dichloro-4-methoxyphenylthio)isovaleric acid as a white crystalline powder mp 176.5°-178.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436748 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-6d83feeed87648da8cc4bc3b1fc68116 |
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| Source note | uspto-grants-1984_03 |
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