HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → 1,5-Dichloro-3-methoxy-2-(2-nitrovinyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 2,4-Dichloro-6-methoxybenzaldehyde | HCID 12802880 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,5-Dichloro-3-methoxy-2-(2-nitrovinyl)benzene | HCID 67080898 | — |
Reaction Steps
A suspension of 2,4-dichloro-6-methoxybenzaldehyde (0.51 g; 2.5 mmol), methylamine hydrochloride (0.11 g; 1.6 mmol) and sodium acetate (0.13 g; 1.6 mmol) in 3 mL of nitromethane was stirred at ambient temperature. After stirring for 15.5 hours the mixture was diluted with 20 mL water and 40 mL DCM, and then transferred to a separatory funnel. After shaking, the organic layer was dried over sodium sulfate and evaporated to give 0.57 g of 1,5-dichloro-3-methoxy-2-(2-nitrovinyl)benzene as a light yellow solid. MS (apci, neg) m/z=247
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569522B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-ffb8872d5dd5419ab1005a8ae1ecbd4b |
| Source note | uspto-grants-2013_10 |