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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032392Generated: November 2, 2026

Water → 2-(3,4-dihydro-2H-1-benzopyran-3-yl)ethan-1-ol

https://huagongshe.com/reaction/1032392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant3-MethoxycarbonylmethylchromanHCID 14838413—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(3,4-dihydro-2H-1-benzopyran-3-yl)ethan-1-olHCID 14838414100%

Reaction Steps

At room temperature and while stirring, a solution of 7.22 g (35 mmol) of 3-methoxycarbonylmethylchroman in 50 ml of absolute tetrahydrofuran is added dropwise within a period of 30 minutes to a suspension of 1.33 g (35 mmol) of lithium aluminium hydride in 50 ml of absolute diethyl ether. Stirring is continued at room temperature for a further 16 hours and then the whole is carefully decomposed with 1.33 ml of water, 1.33 ml of sodium hydroxide solution (15% strength) and 4.0 ml of water. The precipitate formed is filtered off with suction and the filtrate is concentrated by evaporation in vacuo. The oily residue is dissolved in diethyl ether. The solution is washed with water, dried over sodium sulphate and concentrated by evaporation in vacuo. 6.23 g (100%) of 3-(2-hydroxyethyl)chroman are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957928
Source datasetuspto-grants-1990_09
ORD IDord-b9f26cf967564b42a3cdc812ac484dbe
Source noteuspto-grants-1990_09