HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614120Generated: October 25, 2026
Water → Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)-
https://huagongshe.com/reaction/614120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3,5-Bis(phenylmethoxy)benzoic acid | HCID 99307 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethanone, 1-(3,5-bis(phenylmethoxy)phenyl)- | HCID 120098 | — |
Reaction Steps
Over a period of 1.5 hours, methyl lithium (531 ml. of a 2 molar solution, 1.06 M) is added under a nitrogen atmosphere to a rapidly stirring solution of 3,5-dibenzyloxybenzoic acid (175 g., 0.532 M) in ether (250 ml.) - tetrahydrofuran (1400 ml.) maintained at 15°-20° C. After stirring an additional 0.75 hour at 10°-15° C., water (600 ml.) is slowly added keeping the reaction temperature below 20° C. The aqueous layer is separated and extracted with ether (3 × 250 ml.). The organic phases are combined, washed with saturated sodium chloride solution (4 × 300 ml.), dried over sodium sulfate, and concentrated under vacuum to give an oil which slowly crystallized from isopropylether. The crude product is recrystallized from ether-hexane to yield 104.7 g. (59%) of product; m.p. 59°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04143139 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-0678c11daacf45199467e5ec8dda7022 |
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| Source note | uspto-grants-1979_03 |
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