HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 3-(1-(Benzyloxyimino)ethyl)benzylalcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(1-(Benzyloxyimino)ethyl)benzaldehyde | HCID 73433317 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-(Benzyloxyimino)ethyl)benzylalcohol | HCID 86758630 | 96.5% |
Reaction Steps
To a solution of 9.92 g (39.17 mmol) of 3-(1-(benzyloxyimino)ethyl)benzaldehyde in 70 ml of dry methanol and 70 ml of dry tetrahydrofuran was added 1.81 g (43 mmol) of sodium borohydride portionwise with ice-cooling, and the mixture was stirred for 2 hours with ice-cooling. Further, 0.30 g of sodium borohydride portionwise was added thereto with ice-cooling, and the mixture was stirred for 2 hours with ice-cooling. The reaction mixture was poured into 500 ml of an about 5% aqueous solution of ammonium chloride, and the mixture was extracted with tert-butyl methyl ether. The organic layer was dried and concentrated to obtain 9.64 g (37.8 mmol) of 3-(1-(benzyloxyimino)ethyl)benzylalcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06489487B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-565bdc0af0c14cd8850cc433c1c28e52 |
| Source note | uspto-grants-2002_12 |