Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245313Generated: October 28, 2026

Thionyl Chloride → HCID 57831213, compound

https://huagongshe.com/reaction/2245313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13102467HCID 13102467—
CatalystPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 57831213HCID 57831213—

Reaction Steps

A stirred solution of 4.0 grams (0.02 mole) of (4-pyrimidin-2-yloxyphenyl)methanol (known compound) and seven drops of pyridine in 35 mL of methylene chloride was cooled in an ice-water bath and a solution of 2.0 mL (0.027 mole) of thionyl chloride was added dropwise. Upon completion of addition the reaction mixture was stirred at about 10° C. to 20° C. during a three-hour period. After this time, the reaction mixture was poured into a cold aqueous solution of sodium bicarbonate. The mixture was then stirred for 30 minutes and the organic layer was separated. The aqueous layer was extracted with one 50 mL portion of methylene chloride. The extract was combined with the organic layer, and the combination was passed through silicone-coated filter paper to remove traces of water. The filtrate was concentrated under reduced pressure, yielding grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683070B2
Source datasetuspto-grants-2010_03
ORD IDord-8e94b8b7cbc24598b9f4725f3e661af4
Source noteuspto-grants-2010_03