HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085068Generated: October 26, 2026
Ethyl Acetate → Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate
https://huagongshe.com/reaction/2085068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-(3-Methoxyphenyl)-1-phenylethan-1-one | HCID 2759614 | — |
| Reactant | Lithium bis(trimethylsilyl)amide | HCID 57426343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate | HCID 22602685 | 86% |
Reaction Steps
Lithium hexamethyldisilazane (88.5 mL, 88.5 mmol) was added to THF (150 mL) at −78° C. After 15 min, ethyl acetate (7.79 g, 88.5 mmol) was added over 10 min and stirred at −78° C. for 30 min. The m-methoxybenzyl phenyl ketone in (10.0 g, 44.25 mmol) THF (100 mL) was added over 15 min and kept at that temperature for 3 h. The reaction mixture was quenched at that temperature with saturated ammonium chloride (15 mL). The reaction mixture was diluted with ether (200 mL) and the organic layer was washed with brine, (100 mL), dried and was concentrated to afford 12 g (86%) of the desired product. 1H NMR (CDCl3) δ 7.10-7.37 (m, 6H), 6.71-6.74 (m, 1H), 6.60-6.62 (m, 1H), 6.48 (s, 1H), 3.95-4.00 (m, 2H), 3.67 (s, 3H), 2.72-3.07 (m, 4H), 1.06 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06720315B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-b0ac14b7b23a42e38c2e0515707bd6fa |
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| Source note | uspto-grants-2004_04 |
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