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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491631Generated: October 25, 2026

Hydrochloric Acid → (S)-2-[[(2,6-dichloro-3-nitrophenyl)methyl]amino]propanamide

https://huagongshe.com/reaction/1491631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium AcetateHCID 517045—
Reactant2,6-Dichloro-3-nitrobenzaldehydeHCID 2794912—
ReactantL-Alaninamide--hydrogen bromide (1/1)HCID 18632422—
ReactantSodium cyanoborohydride [MI]HCID 20587905—
SolventMethanolHCID 887—
Product(S)-2-[[(2,6-dichloro-3-nitrophenyl)methyl]amino]propanamideHCID 997155270.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371079
Source datasetuspto-grants-1994_12
ORD IDord-1b7705a64d1b4c8e9c75443c68df2631
Source noteuspto-grants-1994_12