HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 7-(4-(tert-butoxycarbonyl)-2-nitrophenoxy)-6,8-dichlorochroman-4-carboxylate → Ethyl 7-(2-amino-4-(tert-butoxycarbonyl)phenoxy)-6,8-dichlorochroman-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 7-(4-(tert-butoxycarbonyl)-2-nitrophenoxy)-6,8-dichlorochroman-4-carboxylate | HCID 67080485 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | Ethyl 7-(2-amino-4-(tert-butoxycarbonyl)phenoxy)-6,8-dichlorochroman-4-carboxylate | HCID 67080422 | 86.5% |
Reaction Steps
To a mixture of ethyl 7-(4-(tert-butoxycarbonyl)-2-nitrophenoxy)-6,8-dichlorochroman-4-carboxylate (2.70 g, 5.27 mmol) in 25 mL of THF and 25 mL of saturated ammonium chloride was added zinc dust (3.45 g, 52.7 mmol) under argon. After 1 hour at ambient temperature, the reaction was diluted with ethyl acetate and filtered. The biphasic filtrate was separated and the organic layer was washed with brine. The organic layer was dried over sodium sulfate, filtered and concentrated. The crude product was dissolved in dichloromethane, concentrated onto silica gel and purified by flash column chromatography, eluting with 20% ethyl acetate in hexanes to give ethyl the desired product (2.20 g, 86.5% yield) as a white foam. MS (ESI) m/z=482 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785445B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-f0b7688b589b42e19f82cd77c0fdfeba |
| Source note | uspto-grants-2014_07 |