HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725254Generated: November 2, 2026
HCID 86599513, compound → HCID 11307773, compound
https://huagongshe.com/reaction/1725254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86599513 | HCID 86599513 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Lithium Hydroxide | HCID 3939 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11307773 | HCID 11307773 | 46% |
Reaction Steps
To a solution of ethyl(2S)-3-[4-(2-{bis[4-(trifluoromethyl)benzyl]amino}-2-oxoethoxy)phenyl]-2-ethoxypropanoate (0.662 g, 1.1 mmol) in acetonitrile (54 mL) was added aqueous 0.10 M LiOH (27 mL) and the solution was stirred at room temperature overnight. The solvent volume was reduced in vacuo and the remaining aqueous phase was diluted with water and aqueous 0.10 M LiOH (to a total volume of 300 mL, pH˜12) and washed with diethyl ether (2×100 mL). (The extraction process was complicated by the formation of emulsions.) The aqueous phase was acidified with 2 M HCl and extracted with ethyl acetate (3×100 mL). The combined organic phase was washed with brine (100 mL), dried over Na2SO4, and concentrated in vacuo to afford 0.292 g (46%) of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488844B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-3b01a1cecff64328adaa4732c6f2e01f |
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| Source note | uspto-grants-2009_02 |
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