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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248417Generated: October 31, 2026

HCID 19763616, compound → HCID 19763623, compound

https://huagongshe.com/reaction/248417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19763616HCID 19763616—
SolventAcetic AcidHCID 176—
ProductHCID 19763623HCID 19763623—

Reaction Steps

The oily residue obtained in stage a) is then heated in toluene (100 cc) and butanol (200 cc) in the presence of paratoluenesulphonic acid (0.5 g), with the separation of the water formed. After evaporating the reaction medium, the residue is chromatographed on a silica column (40:60 ethyl acetate/heptane eluant) to obtain a colourless oil (14.5 g) corresponding to a mixture of alcohol diastereoisomers, namely 2-(2,4-dichlorophenyl)-4-hydroxy-2-chloromethyltetrahydrofuran. This product is directly oxidized with chromic anhydride in acetic acid to obtain, after purification by silica column chromatography, furanone in the form of white crystals, m.p. 99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210198
Source datasetuspto-grants-1993_05
ORD IDord-93769233ea1a4b3db2046687f2096af4
Source noteuspto-grants-1993_05