HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388585Generated: November 3, 2026
Water → 4-[(2,3-Dihydro-1H-inden-2-yl)sulfanyl]phenol
https://huagongshe.com/reaction/1388585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 576069 | HCID 576069 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[(2,3-Dihydro-1H-inden-2-yl)sulfanyl]phenol | HCID 20471397 | — |
Reaction Steps
A solution of 2-(p-methoxyphenylthio) indane (5 g) in dry dichloromethane (40 ml) was cooled to -70°. Boron tribromide (6 g) was added slowly with stirring at -70°. When addition was complete, the reaction mixture was kept at -70° for a further 10 minutes and then allowed to warm to room temperature. The mixture was left overnight and water (70 ml) then added slowly with stirring. The mixture was then poured into water (65 ml) and a further quantity (95 ml) of dichloromethane added, and the mixture agitated. The dichloromethane solution was separated and extracted with 2 molar sodium hydroxide. The cloudy extract was allowed to stand until it cleared and was then decanted from a residue. The solution was acidified with dilute hydrochloric acid and extracted with ether. The ether solution was washed with water, dried, and evaporated to give 2-(p-hydroxyphenylthio)indane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04431834 |
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| Source dataset | uspto-grants-1984_02 |
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| ORD ID | ord-c38ad78c21cc46d5af7ab437854db6eb |
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| Source note | uspto-grants-1984_02 |
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