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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Benzyloxy-5-(4-fluorophenoxy)-1-pentene | HCID 21317658 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyloxy-5-(4-fluorophenoxy)-1-pentanol | HCID 21317584 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04066675 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-39a1f5ec1c93461d8334157f0165df08 |
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| Source note | uspto-grants-1978_01 |
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