HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2-(2,4-Dichlorophenoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,4-Dichloro-1-(2-nitrophenoxy)benzene | HCID 775975 | — |
| Product | 2-(2,4-Dichlorophenoxy)aniline | HCID 96829 | 99% |
Reaction Steps
To a stirred solution of 2,4-dichloro-1-(2-nitro-phenoxy)-benzene (3.5 g, 12.32 mmol) in ethyl acetate (60 mL) stannous chloride dihydrate (13.89 g, 61.6 mmol) was added and the mixture was refluxed for 2 h before it was quenched with saturated sodium hydrogencarbonate solution (192 mL). The organic phase was separated and the aqueous phase was washed several times with ethyl acetate. The combined extracts were dried over sodium sulfate, filtered and concentrated in vacuo to yield 3.1 g (99%) of the title compound as a yellowish oil: MS (EI) 255.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481527B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-4b43fd7ea4a54bb6a4047344a38d7ff1 |
| Source note | uspto-grants-2013_07 |