HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259905Generated: October 31, 2026
Hydrochloric Acid → HCID 57020529, compound
https://huagongshe.com/reaction/259905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10874813 | HCID 10874813 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57020529 | HCID 57020529 | 89.7% |
Reaction Steps
(2S,5S)-2-(N,N-Dibenzylamino)-5-acetylamino-1,6-diphenyl-3-hexanone (3.0 g, 5.944 mmol) was dissolved in methanol (15 ml). Sodium borohydride (1.80 g, 23.78 mmol) was slowly added to the resultant solution while chilling with ice water so as not to raise the temperature above 10° C., thereby conducting reaction. The reaction mixture was stirred at room temperature for 5 hours. To the reaction mixture, was added a 10% hydrochloric acid (10 ml) while chilling with ice water. After bubbling ceased, the mixture was extracted with ethyl acetate (50 ml). The extract was washed with an aqueous sodium chloride and dried over sodium sulfate. The solvent was distilled off, and the resulting crude product was recrystallized from a mixed solvent of ethyl acetate (1.5 ml) and n-hexane (6 ml), thereby obtaining the title compound (2.70 g, 86.1%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05523458 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-8d743006f7cd44e1be436e1ea203d258 |
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| Source note | uspto-grants-1996_06 |
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