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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-Chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methanolHCID 117820924—
SolventDichloromethaneHCID 6344—
Product(2-Chloro-6-(1-ethoxyvinyl)pyrimidin-4-yl)methyl methanesulfonateHCID 117821115108.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09439904B2
Source datasetuspto-grants-2016_09
ORD IDord-40593e2a0654432e8c3879c3a0bc7659
Source noteuspto-grants-2016_09