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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268216Generated: October 30, 2026

Tetrahydrofuran → HCID 70214617, compound

https://huagongshe.com/reaction/2268216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57230451HCID 57230451—
SolventWaterHCID 962—
ProductHCID 70214617HCID 70214617—

Reaction Steps

3.1 g (8.5 mmol) of 4-[3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)acryloyloxy]benzaldehyde and 50 ml of a mixture of THF and methanol (50/50) are introduced into a round-bottomed flask. 163 mg (4.25 mmol) of sodium borohydride is added portionwise and the mixture is stirred at [lacuna] temperature for three hours. The reaction medium is poured into water and extracted with ethyl ether, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate, filtered and evaporated. The solid obtained is recrystallized from a mixture of diisopropyl ether and hexane. After filtration and drying, 1.6 g (53%) of 4-[3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)acryloyloxy]benzenemethanol, with a melting point of 140-50° C., are collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326510B1
Source datasetuspto-grants-2001_12
ORD IDord-d36a83075ffe494299370eaf8c296171
Source noteuspto-grants-2001_12