HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522718Generated: October 25, 2026
Methanesulfonyl chloride → (1-Methylcyclopropyl)methyl methanesulfonate
https://huagongshe.com/reaction/522718
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (1-Methylcyclopropyl)methanol | HCID 137701 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-Methylcyclopropyl)methyl methanesulfonate | HCID 13638452 | 96% |
Reaction Steps
Treat a cooled solution (0° C.) of 1-methylcyclopropanemethanol (2.0 g, 23.22 mmol) in DCM (75 mL) with TEA (2.58 g, 25.5 mmol) and add methanesulfonyl chloride (2.93 g, 25.5 mmol) dropwise. Stir the mixture at 0° C. for 2 h, wash with H2O then brine, dry over Na2SO4 and concentrate to dryness to afford the title compound (3.66 g, 96%) as an oil. 1H NMR (400 MHz, DMSO-d6): δ 3.60 (s, 3H), 2.10 (m, 2H), 0.72 (s, 3H), 0.14 (m, 2H), 0.01 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334267B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8f9522bda5f74728bf876b0552e60e0f |
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| Source note | uspto-grants-2016_05 |
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