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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265156Generated: October 31, 2026

Chloroform → HCID 86614354, compound

https://huagongshe.com/reaction/2265156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68427102HCID 68427102—
SolventEthyl AcetateHCID 8857—
ProductHCID 86614354HCID 86614354—

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C. 0.45 mL of triethylamine and 0.17 mL of methanesulfonyl chloride were added to chloroform (5 mL) solution of 237 mg of (3SR,4RS)-(1-methyl-4-o-tolylpiperidin-3-yl)-methanol obtained in Production Example 33-1. This was stirred at 0° C. for 50 minutes, diluted with ethyl acetate, washed with aqueous saturated sodium hydrogencarbonate solution, and dried with anhydrous sodium sulfate, and the solvent was evaporated off under reduced pressure to obtain 321 mg of 1-methyl-4-o-tolylpiperidin-3-ylmethyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855294B2
Source datasetuspto-grants-2010_12
ORD IDord-a520eae66a89492fb0f40942592ad8f2
Source noteuspto-grants-2010_12