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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729137Generated: October 31, 2026

Tetrahydrofuran → HCID 14549129, compound

https://huagongshe.com/reaction/1729137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14597215HCID 14597215—
SolventEthanolHCID 702—
ProductHCID 14549129HCID 1454912999%

Reaction Steps

33.0 g (0.1 mol) of benzyl 4'-acetyl-4-biphenylcarboxylate, 200 ml of tetrahydrofuran and 50 ml of ethanol were supplied into the same flask as used in Example 9. Then 3.8 g (0.1 mol) of sodium borohydride was added at 15°-25° C. over a period of 10 minutes. After standing at the same temperature for 2 hours, the reaction solution was poured into ice-water and extracted twice with 300 ml of chloroform. The organic layer was washed with water and concentrated under reduced pressure to obtain 32.9 g (99% yield) of benzyl 4'-(1-hydroxyethyl)-4-biphenylcarboxylate (III-15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05332675
Source datasetuspto-grants-1994_07
ORD IDord-892cde5ab1884c9cac52dae692cb2652
Source noteuspto-grants-1994_07