HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 87829163, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18448755 | HCID 18448755 | — |
| Catalyst | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 87829163 | HCID 87829163 | — |
Reaction Steps
3,5-Dichloro-4-(4-amino-3-nitrophenoxy)phenylacetic acid (50 mg), methanol (20 mL) and thionyl chloride (2 drops) was heated at reflux for two hours. After cooling down to room temperature, the reaction mixture was partioned between an aqueous solution of sodium hydrogencarbonate (saturated) and ethyl acetate. The organic phase was washed with brine and concentrated. This gave 45 mg of methyl(3,5-dichloro-4-(4-amino-3-nitro-phenoxy)phenyl) acetate which was reduced using the method described in Example 1(f), to give 40 mg of methyl(3,5-dichloro-4-(3,4-diaminophenoxy)phenyl) acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199265B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-54b417ab2eeb47d39c1b658cf3e0763b |
| Source note | uspto-grants-2007_04 |