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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327867Generated: October 31, 2026

Tetrahydrofuran → HCID 14496321, compound

https://huagongshe.com/reaction/327867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14512984HCID 14512984—
SolventMethanolHCID 887—
ProductHCID 14496321HCID 1449632196.5%

Reaction Steps

120.9 g (0.4 mol) of 4'-acetyl-4-benzyloxybiphenyl, 400 ml of tetrahydrofuran and 100 ml of methanol were supplied into a four-necked flask equipped with a stirrer and a thermometer. Then 15.14 g (0.4 mol) of sodium borohydride was added at 15°-25° C. over a period of 2 hours. The mixture was kept at the same temperature for 5 hours, then poured into ice-water and extracted twice with 500 ml of chloroform. The organic layer was concentrated under reduced pressure to obtain 117.4 g of 4-benzyloxy-4'-(1-hydroxyethyl)biphenyl in a 96.5% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05274168
Source datasetuspto-grants-1993_12
ORD IDord-523a8279df704d92938dc521852c536c
Source noteuspto-grants-1993_12