HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → alpha-(Aminomethyl)-4-methoxybenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Amino-4'-methoxyacetophenone hydrochloride | HCID 12487188 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-(Aminomethyl)-4-methoxybenzyl alcohol | HCID 3016949 | 57.9% |
Reaction Steps
2-Amino-4′-methoxyacetophenone hydrochloride (500 mg) was dissolved in methanol (10 ml), the solution was added with sodium borohydride (188 mg), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was added with sodium borohydride (188 mg), and further stirred for 30 minutes. The reaction mixture was added with 5 N aqueous sodium hydroxide (1 ml), the mixture was stirred for 10 minutes, and then added with chloroform, and the layers were separated. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered, and then the filtrate was concentrated under reduced pressure to obtain the title compound (240 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097708B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-c6b127e9f82f4e08aac86305eb34754b |
| Source note | uspto-grants-2012_01 |