HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Hydroxy-3-(2-nitrophenyl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-(2-Nitrophenyl)-2-oxopropanoic acid | HCID 79583 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | 1-Decanol | HCID 8174 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-3-(2-nitrophenyl)propanoic acid | HCID 13651758 | — |
Reaction Steps
To a magnetically stirred suspension of α-oxo-2-nitrobenzenepropanoic acid (5.00 g) in water (75 ml) containing 1 drop of decyl alcohol was added sodium borohydride (2.50 g) in portions to maintain a temperature between 45 and 50°. The resulting solution was then left at room temperature for 21/2 hours. The solution was acidified with concentrated hydrochloric acid and seeded. Stirring and cooling gave crude product; yield 5.01 g, m.p. 84°-90°. Recrystallization from water gave titled product; yield 2.63 g (52%), m.p. 95°-98° with spectral data as above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04785118 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-4224cee26e49497da19e00baeefb0f90 |
| Source note | uspto-grants-1988_11 |