HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → Benzyl Alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethylene Glycol Monoethyl Ether | HCID 8146 | — |
| Reactant | N-Methylbenzamide | HCID 11954 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Benzyl Alcohol | HCID 244 | — |
| Product | N-Methylbenzylamine | HCID 7669 | — |
Reaction Steps
29.8 g (0.222 mole) of ethyl carbitol was added dropwise to a mixture consisting of 2.8 g (0.074 mole) of sodium borohydride, 5 g (0.037 mole) of N-methyl benzamide and 25 ml of xylene at 120° C. over two hours. Subsequently, the mixture was agitated at the same temperature for 40 hours. After cooling to room temperature, the mixture was neutralized with dilute sulfuric acid. As a result, N-methyl benzylamine was obtained in 67.5% yield and benzyl alcohol in 7.7% yield, respectively. 23.6% of N-methyl benzamide was remained unreactive.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196601 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-ad65dd5e969544989c9e38216d1a3295 |
| Source note | uspto-grants-1993_03 |