HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl isocyanate → ethyl 2-(1-Methyl-2-(benzylcarbamoyl)hydrazinyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl isocyanate | HCID 76639 | — |
| Reactant | Ethyl 2-(1-methylhydrazinyl)acetate | HCID 20288078 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl 2-(1-Methyl-2-(benzylcarbamoyl)hydrazinyl)acetate | HCID 66977957 | 76% |
Reaction Steps
To a solution of ethyl 2-(1-methylhydrazinyl)acetate (Compound XL-1) 10 ml (76 mmol) in tetrahydrofuran 40 ml, benzyl isocyanate 11.1 g (83.3 mmol) was added at 0° C. and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate 150 ml and washed with water 75 ml and brine 75 ml. The organic phase was dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo to obtain the title compound 15.2 g (76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040531B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-e456841d45a84c60b5e7cea3ed743214 |
| Source note | uspto-grants-2015_05 |