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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704160Generated: October 30, 2026

Tetrahydrofuran → HCID 14496321, compound

https://huagongshe.com/reaction/704160

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-benzyloxy-4'-acetylbiphenyl, 400 ml of tetrahydrofuran and 100 ml of methanol were supplied into a four-necked flask provided 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 (96.5% yield) or 4-benzyloxy-4'-(1-hydroxyethyl)-biphenyl (VI-12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985590
Source datasetuspto-grants-1991_01
ORD IDord-6fd79f4b2f2e43f0850e9d4cc6bdc4ee
Source noteuspto-grants-1991_01