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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482386Generated: October 30, 2026

Water → Methyl 2-(2-chloromethyl-5-methylphenoxy)propionate

https://huagongshe.com/reaction/482386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
ReactantMethyl 2-(2-hydroxymethyl-5-methylphenoxy)propionateHCID 23286418—
CatalystPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(2-chloromethyl-5-methylphenoxy)propionateHCID 15765398—

Reaction Steps

A solution of 2.20 g (0.0098 mole) of methyl 2-(2-hydroxymethyl-5-methylphenoxy)propionate in 10 mL of dry methylene chloride was added to a colorless solution of 1.28 g (0.0108 mole) of thionyl chloride and 5 drops of pyridine in 10 mL of dry methylene chloride during a 10 minute period. This mixture was heated at reflux for one hour and then poured into 50 mL of water. The phases were separated, and the aqueous phase was extracted three times with methylene chloride. These extracts were combined with the organic phase, which was then washed three times with a saturated aqueous solution of sodium bicarbonate and once with a saturated aqueous solution of sodium chloride. The organic phase was then dried over anhydrous magnesium sulfate, filtered, and the filtrate was evaporated under reduced pressure, leaving a yellow oil as a residue. This oil was placed on a silica gel column and eluted with methylene chloride. After the product-containing fractions were combined and the solvent evaporated under reduced pressure, 2.06 g of methyl 2-(2-chloromethyl-5-methylphenoxy)propionate was recovered as a colorless oil. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798316
Source datasetuspto-grants-1998_08
ORD IDord-a2c361e282924240ac7b1f18905293b9
Source noteuspto-grants-1998_08