HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4210Generated: October 27, 2026
Thiophenol → 4-(Phenylsulfanyl)butan-1-ol
https://huagongshe.com/reaction/4210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-1-butanol | HCID 13569 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 4-(Phenylsulfanyl)butan-1-ol | HCID 283798 | 57.8% |
Reaction Steps
A mixture of thiophenol (121.2 g, 1.10 mole), 4-chloro-1-butanol (100.0 g, 0.921 mole), and potassium carbonate (138.2 g, 1.0 mole) was heated overnight at gentle reflux in dimethoxyethane. The reaction mixture was filtered and solvent removed by rotary evaporator. The residue obtained was dissolved in chloroform and extracted with 10% sodium hydroxide. The chloroform layer was dried, filtered, and solvent removed to give an oil which crystallized to a white solid. The solid was vacuum distilled at 134°-140° C./0.55 mm. A six-gram sample of the distilled oil was subjected to flash chromatography on silica gel using ethyl acetate-hexanes for elution. This gave a clear oil which was dried at 80° C. overnight in vacuo. The process produced 5.2 g (57.8%) of clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04724235 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-9b6bca417c434762bad8de93b51a34db |
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| Source note | uspto-grants-1988_02 |
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