HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507793Generated: November 3, 2026
Gamma-Aminobutyric Acid → HCID 123537105, compound
https://huagongshe.com/reaction/507793
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Gamma-Aminobutyric Acid | HCID 119 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 123203838 | HCID 123203838 | — |
| Product | HCID 123537105 | HCID 123537105 | 65% |
Reaction Steps
4-diisopropylsilanylbenzoyl chloride (2) (1.7 g, 6.7 mmol) was added into 1N sodium hydroxide aqueous solution (9 mL) dissolving 4-aminobutanoic acid (910 mg. 8.94 mmol) and stirred for 8 hours. After the addition of 12N hydrochloric acid to the aqueous solution to reach pH 2, the solution was extracted with 400 mL of CH2Cl2 and an organic layer was then collected. The resulting organic layer was dehydrated with anhydrous sodium sulfate and filtered so that the resulting solvent was distilled out under a reduced pressure. A desired compound was then purified by silica gel column chromatography. After eluted with chloroform having 0-3% methanol gradient, the solvent was distilled out to give the desired compound as white solid (1.4 g, 65%). Its NMR data are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786296B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-0a3055462a31423ead7a1f648bd7c078 |
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| Source note | uspto-grants-2010_08 |
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