HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218192Generated: October 30, 2026
Water → 3-Hydroxybutyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/2218192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1,3-Butanediol | HCID 7896 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Hydroxybutyl 4-methylbenzenesulfonate | HCID 13204323 | 57% |
Reaction Steps
Pyridine (9.0 ml, 111 mmol) was added to a solution of 1,3-butanediol (5.07 g, 56.3 mmol) in anhydrous methylene chloride (20 ml) at room temperature. After ice-cooling, p-toluenesulfonyl chloride (15.9 g, 83.4 mmol) was added thereto, the mixture was stirred at room temperature overnight, then water (60 ml) was added to the reaction mixture, and the whole was extracted with ethyl acetate (100 ml). The ethyl acetate layer was washed with 1 N hydrochloric acid (30 ml) and saturated brine (30 ml) successively and dehydrated with anhydrous magnesium sulfate. Ethyl acetate was evaporated under reduced pressure, and the obtained oily matter was purified by silica gel column chromatography (mobile phase:hexane/ethyl acetate=3/1) to give 7.72 g (57%) of the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410987B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-2336f2afaae748e2a6c77c06543e57b3 |
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| Source note | uspto-grants-2008_08 |
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