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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221594Generated: November 3, 2026

Thionyl Chloride → HCID 86605729, compound

https://huagongshe.com/reaction/2221594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86605727HCID 86605727—
SolventTolueneHCID 1140—
ProductHCID 86605729HCID 8660572994%

Reaction Steps

To a mixture of ethyl (3-{4-[(4-hydroxymethyl-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}phenyl)acetate (7.50 g) and toluene (300 mL) was added thionyl chloride (2.38 g), and the mixture was heated under reflux for 1 hr. After concentration of the reaction mixture, saturated aqueous sodium hydrogen carbonate was added to the residue and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated to give ethyl (3-{4-[(4-chloromethyl-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}phenyl)acetate as colorless crystals (7.32 g, yield 94%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 95-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-6ecbaf8340e04a0eafef3c6ad3b212fd
Source noteuspto-grants-2008_05