HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5-(Diethoxymethyl)-3-methoxy-2-nitrothiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Bromo-5-(diethoxymethyl)-2-nitrothiophene | HCID 86703858 | — |
| Product | 5-(Diethoxymethyl)-3-methoxy-2-nitrothiophene | HCID 86703859 | 403.1% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a solution of 3-bromo-5-(diethoxymethyl)-2-nitrothiophene (Int. 66) (1 g, 3.22 mmol) in MeOH (10 ml) copper(II) oxide (0.051 g, 0.645 mmol), KI (10.7 mg, 0.064 mmol) and sodium methanolate (0.662 g, 12.25 mmol) were added, and the mixture was heated under MW irradiation at 120° C. for 2 hours. The reaction mixture was filtered through a celite pad, the filtrate was concentrated under vacuum and then partitioned between 0.5N HCl and EtOAc. The organic phase was dried over sodium sulfate, filtered and evaporated to give 5-(diethoxymethyl)-3-methoxy-2-nitrothiophene (Int. 67) (680 mg, 2.60 mmol, MS/ESI+261.0 [MH]+). This crude was used without any additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440954B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-70e42477b2454f43bc0b4c6e243142dc |
| Source note | uspto-grants-2016_09 |