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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704162Generated: October 29, 2026

Tetrahydrofuran → HCID 14496321, compound

https://huagongshe.com/reaction/704162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 14512984HCID 14512984—
ReactantHCID 178418435HCID 178418435—
SolventMethanolHCID 887—
ProductHCID 14496321HCID 1449632195%

Reaction Steps

12.09 g (0.04 mol) of 4'-acetyl-4-benzyloxybiphenyl (VII-23), 40 ml of tetrahydrofuran and 10 ml of methanol were supplied into a four-necked flask provided with a stirrer and a thermometer. Then 1.51 g (0.4 mol) of sodium boron hydride 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 with 50 ml of chloroform. The organic layer was concentrated under reduced pressure to give 11.0 g (95% yield) of 4-benzyloxy-4'-(1-hydroxyethyl)biphenyl (VI-23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985590
Source datasetuspto-grants-1991_01
ORD IDord-bca63a586eed4d13bad98483664ffcfe
Source noteuspto-grants-1991_01