HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229462Generated: October 25, 2026
Water → (R)-3-hydroxybutyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/2229462
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (-)-1,3-Butanediol | HCID 637497 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (R)-3-hydroxybutyl 4-methylbenzenesulfonate | HCID 13204324 | 89.6% |
Reaction Steps
After adding pyridine (100 ml) to (R)-1,3-butanediol (86.0 g), the solution was cooled to −25° C. under nitrogen atmosphere. A solution of p-toluenesulfonyl chloride (200 g) in pyridine (200 ml) was slowly added dropwise thereto at a temperature ranging from −20 to −10° C. The mixture was stirred for 1 hour at a temperature ranging from −20 to −10° C. A small amount of water was added to the reaction mixture to stop the reaction and the solution was extracted with toluene and water. The organic layer was washed with water, dried over sodium sulfate, and concentrated under reduced pressure to obtain (R)-3-hydroxy-1-(p-toluenesulfonyloxy)butane (209 g) as light brown oil. The oil thus obtained was used in the next step as such without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06420409B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-cdd6798588e847b2a5bc0fcbafb4822d |
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| Source note | uspto-grants-2002_07 |
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