HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715126Generated: October 27, 2026
Methanesulfonyl chloride → (1-Methylcyclopropyl)methyl methanesulfonate
https://huagongshe.com/reaction/715126
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 | 97% |
Reaction Steps
Treat a 0° C. solution of (1-methylcyclopropyl)methanol (1.0 g, 11.61 mmol) in DCM (50 mL) with TEA (1.29 g, 12.77 mmol), add methanesulfonyl chloride (1.46 g, 12.77 mmol) drop-wise and stir at 0° C. for 2 h. Warm the mixture to RT, wash with H2O, then brine, dry over Na2SO4 and concentrate to dryness to afford the title compound (1.85 g, 97%) as an oil. 1H NMR (400 MHz, DMSO-d6): δ 4.05 (s, 2H), 3.20 (s, 3H), 1.17 (s, 3H), 0.59 (m, 2H), 0.47 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187474B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-55dd982daedf406fa2a1f499ad158f9a |
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| Source note | uspto-grants-2015_11 |
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