HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280278Generated: October 30, 2026
Gamma-Aminobutyric Acid → HCID 135674608, compound
https://huagongshe.com/reaction/280278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4',5-Dichloro-2-hydroxy-3-methylbenzophenone | HCID 3021137 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135674608 | HCID 135674608 | — |
Reaction Steps
4-Aminobutanoic acid (2.2 g; 0.0213 mol), sodium methoxide (1.16 g; 0.0213 mol) and (5-chloro-2-hydroxy-3-methylphenyl)-(4-chlorophenyl)-methanone (6 g; 0.0213 mol) are introduced into a mixture of 200 ml of ethanol and 400 ml of methanol, and the resulting mixture is then evaporated to dryness. Ethanol (500 ml) is added to the residue and the mixture is then evaporated to dryness. The latter operation is repeated 4 times. The residue is dissolved in 1 liter of water and the pH is acidified to pH 4 by the addition of citric acid. The precipitate is filtered off, washed with water and then dissolved in CH2Cl2. The organic solution is washed with water, dried (MgSO4) and filtered, and the filtrate is evaporated to give an oil, which is crystallised once from petroleum ether and recrystallised twice from AcOEt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04588748 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-dc723d912eb64682bf767dbedf9e0b22 |
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| Source note | uspto-grants-1986_05 |
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