HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005313Generated: October 29, 2026
Water → Ethyl 3-[4-benzyloxyphenyl]-2-butoxypropanoate
https://huagongshe.com/reaction/1005313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl ester | HCID 15186153 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-[4-benzyloxyphenyl]-2-butoxypropanoate | HCID 21930967 | 20% |
Reaction Steps
A solution of ethyl 3-[4-benzyloxyphenyl)-2-hydroxypropanoate (5.0 g, 16.6 mmol) (prepared in a similar manner as described in Ref: WO95/18125) in dry dimethyl formamide (5 mL) was added to a suspension of sodium hydride (0.1 g, 41.6 mmol) (60% dispersion in oil) in dry dimethyl formamide (3 mL) at 0° C. and stirring was continued for further 1 h. To the above reaction mixture n-butyl bromide (3.4 g, 24.0 mmol) was added at 0° C. and stirring was continued for 10 h at ca. 25° C. Water (30 mL) was added and extracted with ethyl acetate (2×50 mL). The combined ethyl acetate layer was washed with water (50 mL), brine (25 mL), dried (Na2SO4), filtered and the solvent was evaporated. The residue was chromatographed over silica gel using a mixture of ethyl acetate and and pet. ether (1:9) as an eluent to afford the title compound (0.7 g, 20%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054453 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-d3ab6346703e4cfcb41f273d356dac5f |
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| Source note | uspto-grants-2000_04 |
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