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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951986Generated: October 31, 2026

Tetrahydrofuran → HCID 68600087, compound

https://huagongshe.com/reaction/1951986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 68601983HCID 68601983—
ProductHCID 68600087HCID 6860008777%

Reaction Conditions

Temperature60 °C

Reaction Steps

2.4 g (110 mmol) of lithium borohydride is added in portions to a solution of 10.6 g (36.7 mmol) of [3-chloro-4-(2-methoxy-ethoxymethoxy)-phenyl]-methyl acetate diluted in 110 ml of tetrahydrofuran. The reaction mixture is stirred at 60° C. for 2 hours. The reaction mixture is then poured into 500 ml of ice and then extracted with ethyl acetate. The organic phases are combined, washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and evaporated. The solvents are evaporated to give 7.3 g (77%) of 2-[3-chloro-4-(2-methoxy-ethoxymethoxy)-phenyl]-ethanol in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404836B2
Source datasetuspto-grants-2013_03
ORD IDord-5a59e89a49e049acadb75cd2ccd28794
Source noteuspto-grants-2013_03