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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769387Generated: November 1, 2026

Methanol → HCID 15229923, compound

https://huagongshe.com/reaction/1769387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHexaneHCID 8058—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15229921HCID 15229921—
SolventWaterHCID 962—
ProductHCID 15229923HCID 15229923—

Reaction Steps

A mixture of 4.0 g (11.7 mmol) of methyl (E)-6-(1,3-dihydro-4-cyano-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate and 1.86 g (46.5 mmol) of sodium hydroxide in 100 ml of 3:2 water:methanol was heated at reflux for 2 hours. The resulting homogenous solution was distilled until 30 ml of distillate was recovered. An additional 0.6 g (15 mmol) of sodium hydroxide was added to the reaction solution and it was refluxed for 2 days. Upon cooling the solution was partitioned between 1N aqueousHCl and ethyl acetate. The organic phase was washed twice with water, once with brine, and then dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give a solid. This solid was stirred with hexane and then filtered off to give 3.88 g (11.1 mmol) of (E)-6-(1,3-dihydro-4-carboxy-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4hexenoic acid as a white solid, mp 172°-174° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380879
Source datasetuspto-grants-1995_01
ORD IDord-6ee42e1ba0934149ad449304890de66a
Source noteuspto-grants-1995_01