HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568790Generated: October 30, 2026
Hydrochloric Acid → HCID 14076759, compound
https://huagongshe.com/reaction/568790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Alaninol | HCID 80307 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (2,3-Dichlorophenyl)acetaldehyde | HCID 22379768 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14076759 | HCID 14076759 | 48.4% |
Reaction Steps
To a solution of 13.0 g (0.074 mole) of crude 2,3-dichlorobenzeneacetaldehyde in 50 ml of MeOH was added 5.7 ml (0.074 mole) of (S)-2-amino-1-propanol. The reaction was placed under an atmosphere of argon and 3.6 g (0.058 mole) of sodium cyanoborohydride was added. After stirring for 2.5 hr, the reaction was made acidic by adding ethereal hydrogen chloride. After stirring of 30 min enough 3N sodium hydroxide was added to make the reaction basic. The reaction mixture was extracted with ether and the ether layer was washed with water, brine and dried (K2CO3). Evaporation of the solvent in vacuo gave a yellow oil. The oil was treated with ethereal hydrogen chloride and the solid was collected. The solid was recrystallized from 2-propanol to give 5.10 g of the title compound (28% yield), mp 148°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04729994 |
|---|
| Source dataset | uspto-grants-1988_03 |
|---|
| ORD ID | ord-cf25344dc02943c2a3cfbd324f11469e |
|---|
| Source note | uspto-grants-1988_03 |
|---|