HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37415Generated: October 25, 2026
Gamma-Butyrolactone → 4-((3-Bromophenyl)thio)butanoic acid
https://huagongshe.com/reaction/37415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Butyrolactone | HCID 7302 | — |
| Reactant | m-Bromobenzenethiol | HCID 80597 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-((3-Bromophenyl)thio)butanoic acid | HCID 54515419 | — |
Reaction Steps
3.74 g of sodium were dissolved in 77 ml of absolute ethanol under argon. The solution was treated dropwise with 25 g of m-bromothiophenol and heated to reflux. Thereafter, 12.4 ml of γ-butyrolactone were added and the reaction mixture was heated to 110° C. for 5 hours. The separated carboxylic acid sodium salt was removed by filtration, washed with a small amount of ether and dissolved in 300 ml of water. The solution was acidified to pH 2 with 1N HCl while cooling with ice, the free carboxylic acid was extracted with ether, the ethereal solution was dried and evaporated. There were obtained 33.1 g of 4-(m-bromophenylmercapto)butyric acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420273 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-6cb72450fdfa4b8d8d6fea27607b02ae |
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| Source note | uspto-grants-1995_05 |
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