HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326889Generated: October 25, 2026
Hydrochloric Acid → (S)-2-[[(2,6-dichloro-3-nitrophenyl)methyl]amino]propanamide
https://huagongshe.com/reaction/326889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2,6-Dichloro-3-nitrobenzaldehyde | HCID 2794912 | — |
| Reactant | L-Alaninamide--hydrogen bromide (1/1) | HCID 18632422 | — |
| Reactant | Sodium cyanoborohydride [MI] | HCID 20587905 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-2-[[(2,6-dichloro-3-nitrophenyl)methyl]amino]propanamide | HCID 9971552 | 70.7% |
Reaction Steps
To a homogeneous solution of 8.42 parts of (S)-2-aminopropanamide monohydrobromide, 12.26 parts of sodium acetate and 79 parts of methanol there were added 10.96 parts of 2,6-dichloro-3-nitrobenzaldehyde and, after 1/2 hour, a mixture of 3.77 parts of sodium cyanotrihydroborate and 7.9 parts of methanol. The whole was stirred for 45 min at room temperature. After acidifying to pH 1 with HCl (3N), stirring was continued overnight. The reaction mixture was evaporated and the residue was basified with NaHCO3 (sat.). The product was extracted with dichloromethane and the extract was dried, filtered and evaporated. The residue was recrystallized from 2-propanol, yielding 10.29 parts (70.7%) of (S)-2-[[(2,6-dichloro-3-nitrophenyl)methyl]amino]propanamide (interm. 69).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270464 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-1381cb406f7a48efa44f4b31bfca75af |
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| Source note | uspto-grants-1993_12 |
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