HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20289613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 20289612 | HCID 20289612 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20289613 | HCID 20289613 | — |
Reaction Steps
4 g of 2-Formyl-5-methoxy-4-biphenylacetic acid are dissolved in 300 ml of dry tetrahydrofuran and 2.5 g of sodium borohydride added. The reaction mixture is warmed to 80° for 40 minutes and, after cooling, dropped onto 150 g of ice, acidified with 2 N hydrochloric acid and extracted three times with ethyl acetate. The organic phases are washed with saturated brine, dried over Na2SO4 and concentrated. The residue is hydrogenated in 200 ml of ethyl acetate in the presence of 250 mg of Pd (10% on active charcoal) at a hydrogen pressure of 2 atmospheres. After three hours, the reaction mixture is filtered through talc and the filtrate evaporated. The product is recrystallized from ethyl acetate. M. pt. 127°-128°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04252817 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-309d8e433d0945d29e9ec23cbe9aa075 |
| Source note | uspto-grants-1981_02 |