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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833479Generated: October 31, 2026

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

https://huagongshe.com/reaction/1833479

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, 4 ml.) 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 numberUS04066675
Source datasetuspto-grants-1978_01
ORD IDord-39a1f5ec1c93461d8334157f0165df08
Source noteuspto-grants-1978_01