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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281632Generated: October 31, 2026

Tetrahydrophthalic anhydride → (Cyclohex-4-ene-1,2-diyl)dimethanol

https://huagongshe.com/reaction/1281632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrophthalic anhydrideHCID 6810—
ReactantPotassium Sodium TartrateHCID 9357—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(Cyclohex-4-ene-1,2-diyl)dimethanolHCID 32510082%

Reaction Steps

A solution of one hundred (100) parts by weight of a 1,2,3,6-tetrahydrophthalic anhydride in 500 parts of dry tetrahydrofuran is slowly added to a stirring mixture of 28.75 parts of lithium aluminum hydride and 162 parts of tetrahydrofuran. After the addition is complete, the mixture is refluxed for 24 hours. It is then hydrolyzed by a slow addition of a saturated Rochelle salt solution until it turns white. The mixture is refluxed for an additional 10 hours, allowed to room temperature, and suction filtered. The solvent is removed by a distillation and the viscous liquid crude product is purified by a fractional distillation under vacuum (yield 82%. b.p.: 165-170° C. at 12 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06454965B1
Source datasetuspto-grants-2002_09
ORD IDord-0544a4762f92461da53c36664d4a730a
Source noteuspto-grants-2002_09