HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417338Generated: October 25, 2026
Water → 3-(Methylsulfonyl)propyl methanesulfonate
https://huagongshe.com/reaction/417338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-(Methylsulfonyl)-1-propanol | HCID 200424 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Methylsulfonyl)propyl methanesulfonate | HCID 10262758 | 90% |
Reaction Steps
Step A To a solution of 3-methanesulfonyl-propan-1-ol (Cambridge) (0.5 g, 3.6 mmol) in dichloromethane (3 mL) at 0° C. was added triethylamine (0.5 g, 5 mmol), and methanesulfonyl chloride (0.3 mL, 4 mmol, Aldrich). The reaction mixture was stirred at 0° C. for 2 h. The mixture was poured into water, extracted with dichloromethane. The organic layer was separated, washed with water, brine, dried over MgSO4, and concentrated to give crude methanesulfonic acid 3-methanesulfonyl-propyl ester as a yellow oil (Yield 0.7 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088815B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-f0bbd623ad704d3fb4e1c7c6bfa3c612 |
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| Source note | uspto-grants-2012_01 |
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