HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822803Generated: November 1, 2026
Tetrahydrofurfuryl alcohol → (Tetrahydrofuran-2-yl)methyl methanesulfonate
https://huagongshe.com/reaction/1822803
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (Tetrahydrofuran-2-yl)methyl methanesulfonate | HCID 266119 | 92% |
Reaction Steps
Tetrahydrofurfuryl alcohol (2.01 g, 19.7 mmol, 1.0 eq.) was dissolved in dichloromethane (100 mL) under an argon atmosphere, cooled to 0° C. and treated sequentially with triethylamine (3.02 mL, 21.7 mmol, 1.1 eq) and methanesulfonyl chloride (1.60 mL, 20.7 mmol, 1.05 eq.). The ice bath was removed and stirring continued for 14 h before the mixture was poured into a separatory funnel containing water. The phases were separated and the organic layer was washed with water (4×), dried on MgSO4, filtered and concentrated in vacuo to yield 3.26 g [92%] of tetrahydrofurfuryl methanesulfonate as a crude pale yellow oil, used in the subsequent displacement step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037916B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-72aac5e214b64d28bf5983b6320d93b9 |
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| Source note | uspto-grants-2006_05 |
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