HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium hydroxide, monohydrate → 2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | ethyl 2-(1-Methyl-2-(benzylcarbamoyl)hydrazinyl)acetate | HCID 66977957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methanol tetrahydrofuran water | HCID 21892291 | — |
| Product | 2-(2-(Benzylcarbamoyl)-1-methylhydrazinyl)acetic acid | HCID 53397489 | 88.5% |
Reaction Steps
To a solution of ethyl 2-(1-methyl-2-(benzylcarbamoyl)hydrazinyl)acetate (Compound XXXII-1) 1.33 g (5.0 mmol) in tetrahydrofuran/methanol/water (2:3:1) 24 ml, lithium hydroxide monohydrate 420 mg (10.0 mmol) was added and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with water 25 ml and washed with ether 25 ml. The aqueous phase was acidified with 10%-citric acid 25 ml and extracted with chloroform 30 ml. The organic phase was washed with brine 25 ml and dried with magnesium sulfate and then filtered. The filtrate was concentrated in vacuo to obtain the title compound 1.05 g (88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040531B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-44dbb38d3e9c442083f9b24f2ebb3a23 |
| Source note | uspto-grants-2015_05 |