HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337230Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86674089, compound
https://huagongshe.com/reaction/337230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 64793016 | HCID 64793016 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86674089 | HCID 86674089 | 89.1% |
Reaction Steps
Diisopropylethylamine (0.19 ml, 1.17 mmol) was added to a cool (0° C.) solution of (4-Hydroxymethyl-phenyl)-carbamic acid benzyl ester (0.25 g, 0.97 mmol) in DCM (8 ml) and the reaction stirred at this temperature for 5 minutes. After this time, methane sulfonyl chloride (0.09 ml, 1.07 mmol) was added dropwise and the mixture was allowed to warm to room temperature and stirred for 1 hour. The reaction mixture was then diluted with DCM (20 ml) and washed sequentially with saturated sodium bicarbonate solution (10 ml), saturated ammonium chloride (10 ml) and brine (10 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated to afford the title compound (0.29 g, 89% yield) as a yellow oil which was taken forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889716B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3a55568aabed4e3390eb1e20ccdc0448 |
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| Source note | uspto-grants-2014_11 |
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