HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59078Generated: October 27, 2026
Methanesulfonyl chloride → (2-Chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methyl methanesulfonate
https://huagongshe.com/reaction/59078
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2-Chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methanol | HCID 117820924 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-Chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methyl methanesulfonate | HCID 117821115 | 108.3% |
Reaction Steps
Methanesulfonyl chloride (0.369 mL, 4.73 mmol) was added to an ice-cold solution of (2-chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methanol (846 mg, 3.94 mmol) in DCM (8 mL) containing N,N-diisopropylethylamine (1.0 mL, 5.91 mmol). The mixture was stirred at 0° C. for 10 min. DCM (30 mL) was added and the mixture was washed with water (5 mL). The organic phase was dried over sodium sulfate, filtered and the solvent was evaporated to give the title compound (2-chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methyl methanesulfonate (1249 mg, quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09439904B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-40593e2a0654432e8c3879c3a0bc7659 |
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| Source note | uspto-grants-2016_09 |
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