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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083309Generated: November 1, 2026

Water → 4-Benzyloxy-5-(4-fluorophenoxy)-1-pentanol

https://huagongshe.com/reaction/2083309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Benzyloxy-5-(4-fluorophenoxy)-1-penteneHCID 21317658—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyloxy-5-(4-fluorophenoxy)-1-pentanolHCID 21317584100%

Reaction Steps

To a mixture of 4-benzyloxy-5-(4-fluorophenoxy)-1-pentene (2.86 g., 10 mmoles), sodium borohydride (0.47 g., 12.5 mmoles), and tetrahydrofuran (25 ml.) is added dropwise a solution of boron fluoride etherate (2.1 ml., 16.7 mmoles) in tetrahydrofuran (5 ml.) at ice-bath temperatures under a nitrogen atmosphere. The resulting mixture is further stirred at room temperature overnight (ca. 15 hours). The reaction flask is chilled in an ice bath and water (2 ml.) is very cautiously added to destroy the excess hydride, followed by the additions of sodium hydroxide (5N, 4ml.) and hydrogen peroxide (30%, 8 ml.). The final mixture is stirred at room temperature for one half hour, diluted with cold water and then extracted with chloroform three times. The combined extracts are washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent is evaporated in vacuo leaving the title compound as a viscous oil (3.00 g., 10 mmoles, 100%). ir (neat) 2.97, 3.30, 3.41, 6.22, 6.68, 6.90, 8.03, 8.30, 9.16, 9.44, 12.10, 13.20, 13.60, 14.40μ; pmr (CCl4)δ1.4-1.9 (4H, m), 3.2-4.2 (6H, m), 4.58 (2H, broad s), 6.6-7.1 (4H, m), 7.20 (5H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085125
Source datasetuspto-grants-1978_04
ORD IDord-a85ef28b87e1448bbf4b4a50abb32f26
Source noteuspto-grants-1978_04