HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697761Generated: November 1, 2026
4-Toluenesulfonyl chloride → HCID 86646873, compound
https://huagongshe.com/reaction/1697761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 66771403 | HCID 66771403 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86646873 | HCID 86646873 | 46% |
Reaction Steps
To a solution of 2-(4-Chloro-phenoxy)-4-hydroxy-butyric acid methyl ester (Example 473b), 0.225 g) in dichloromethane (1.88 mL) at room temperature, was added triethylamine (116 mg) and 4-methylbenzene-1-sulfonyl chloride (177 mg). The mixture was stirred at 22° C. for 48 hr. The reaction mixture was partitioned between water and ethyl acetate. The phases were separated. The aqueous layer was extracted with ethyl acetate. The organic layers were washed with brine, dried over Na2SO4 and filtered. The crude mixture was concentrated to dryness and purified by chromatography on silica gel to yield the title compound as a colorless oil (169 mg; 46%). MS (ESI): m/z=419 [M+NH4]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163793B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-97b0a693bcd24643b1ee9ce9536b9614 |
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| Source note | uspto-grants-2012_04 |
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