HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120146Generated: October 30, 2026
Benzene → 2-(S)-amino-3-methyl-1-phenyl-1-pentanone hydrochloride
https://huagongshe.com/reaction/2120146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | L-Isoleucine | HCID 6306 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 2-(S)-amino-3-methyl-1-phenyl-1-pentanone hydrochloride | HCID 18741229 | — |
Reaction Steps
To a stirred suspension of phosphorus pentachloride (31.4 g, 0.151 mmol.) in anhydrous benzene (300 mL) was added L-isoleucine (19.67 g, 0.151 mmol.) under chilling with ice. The mixture was then stirred for 2 hours under chilling with ice, and further stirred for 17 hours at room temperature. The reaction mixture was chilled with ice and anhydrous aluminum chloride (60 g) was portionwise added. The mixture was then slowly heated ed to reflux temperature for a period of 2 hours. The mixture was refluxed for 3 hours, and then chilled with ice. The chilled reaction mixture was slowly added to a mixture of concentrated hydrochloric acid (45 mL) and ice (0-3 kg). The resulting mixture was stirred at 5° C. for 40 min, The precipitated crystals were collected by filtration and washed with benzene. The washed crystals were dried in air to give 2-(S)-amino-3-methyl-1-phenyl-1-pentanone hydrochloride as a white crystalline product (29.2 g, yield! 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689785B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-f30992ba9490470887c2426f38969aad |
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| Source note | uspto-grants-2004_02 |
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