Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457982Generated: October 31, 2026

Thionyl Chloride → HCID 10900314, compound

https://huagongshe.com/reaction/1457982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 11010183HCID 11010183—
SolventPyridineHCID 1049—
ProductHCID 10900314HCID 1090031468%

Reaction Steps

A 90.31 g (0.37 mol) portion of ethyl 1-ethoxycarbonyl-β-hydroxy-β-methyl-cyclopropanepropanoate was dissolved in 182 ml of pyridine to which was subsequently added dropwise thionyl chloride at -10° C. to -5° C. After completion of the dropwise addition, this was stirred at the same temperature for 3 hours. After completion of the reaction, the reaction solution was poured into 1 liter of ice water and extracted with dichloromethane (300 ml×3). The organic layers were combined, washed with 1N hydrochloric acid (1 liter×1) and saturated brine (1 liter×1) in that order and then dried on anhydrous sodium sulfate. To the resulting dichloromethane solution was added dropwise 58 ml of 1,8-diazabicyclo[5,4,0]-7-undecene at 0° C., followed by 18 hours of stirring at room temperature. After completion of the reaction, the reaction solution was washed with 1N hydrochloric acid (1 liter×1) and saturated brine (1 liter×1) in that order, and then dried over anhydrous sodium sulfate. After evaporation of the solvent, the resulting residue was applied to a silica gel column chromatography to yield 56.57 g (68%) of the title compound as an oily substance from the eluate of n-hexane:ethyl acetate=9:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849757
Source datasetuspto-grants-1998_12
ORD IDord-4d9d7940f3234d7986f71dd8e318c557
Source noteuspto-grants-1998_12