HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-amino-5(N-methyl-allyloxycarbamoyl)-benzoic acid allyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Stannous chloride dihydrate | HCID 61436 | — |
| Reactant | 3-(N-methyl-allyloxycarbamoyl)-5-nitro-benzoic acid allyl ester | HCID 22986100 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-amino-5(N-methyl-allyloxycarbamoyl)-benzoic acid allyl ester | HCID 22986141 | 99.6% |
Reaction Steps
A mixture of (8(b)) (0.523 g), tin(II) chloride dihydrate (1.84 g) and ethyl acetate (50 ml) was heated under reflux for 6 hours. The mixture was allowed to cool to ambient temperature and ammonia solution (sp. g. 0.880) was added dropwise until the solution reached pH 8. The white precipitate which had formed was filtered off. washed with ethyl acetate (2×50 ml) and the combined washings and filtrate evaporated to dryness to give the desired starting material (8(c)) as a yellow oil (0.472 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541491B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-831059d1189841e79c57983a6cc92942 |
| Source note | uspto-grants-2003_04 |