HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411143Generated: October 26, 2026
Water → 4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrile
https://huagongshe.com/reaction/411143
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | 4-[1-(3,4-Dimethoxyphenoxy)-3-butenyl]benzonitrile | HCID 21867689 | — |
| Reactant | Sodium;3-oxidodioxaborirane;tetrahydrate | HCID 23693097 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[1-(3,4-Dimethoxyphenoxy)-4-hydroxybutyl]benzonitrile | HCID 21867726 | 78% |
Reaction Steps
Borane-methyl sulfide complex (2 M in ether, 11 mL, 22 mmol) was added dropwise to a cooled (−5° C.) solution of 4-[1-(3,4-dimethoxyphenoxy)-3-butenyl]benzonitrile (from step (i) above; 17.6 g, 56.8 mmol) in dry THF (15 mL) over a period of 15 minutes (during which time the reaction temperature rose to 0° C.). The resulting mixture was stirred at between 0 and 10° C. for 1.5 h, before being allowed to warm to rt. Stirring was continued for a further 3.5 h at this temperature before water (22 mL) and sodium perborate tetrahydrate (11 g, 66 mmol) were added. The biphasic mixture was stirred for 2 h at rt before the water layer was separated and extracted with ether. The combined organic layers were washed with brine, dried and concentrated in vacuo. The resulting residue was purified by chromatography on silica gel, eluting with IPA:ethyl acetate:heptane (5:25:70) to yield 14.5 g (77%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559143B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-a304a75cb385486592cb80fd41eca0f6 |
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| Source note | uspto-grants-2003_05 |
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