Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5-Dimethoxybenzaldehyde | HCID 81747 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Dibromomethane | HCID 3024 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,5-Dimethoxystyrene | HCID 9815298 | 373.9% |
Reaction Steps
Zinc powder (purity; 85%, 14.75 g) is suspended in N,N-dimethylformamide (50 ml) under argon atmosphere, and thereto is added dropwise with stirring acetyl chloride (1.06 g) at 50° C. over a period of 10 minutes, and then the mixture is stirred for 15 minutes. To the mixture is added dropwise a solution of 3,5-dimethoxybenzaldehyde (10 g) in dibromomethane (15.69 g) over a period of 20 minutes, and the mixture is stirred for 30 minutes. The reaction solution is cooled with ice, and thereto is added dropwise a saturated aqueous ammonium chloride solution (40 ml), and further thereto is added diethyl ether. The insoluble materials are removed by filtration, and the filtrate is extracted with diethyl ether. The extract is washed successively with 10% hydrochloric acid, water, 10% aqueous sodium hydroxide solution, and a saturated aqueous sodium chloride solution, dried, and concentrated under reduced pressure to give 3,5-dimethoxystyrene (8.29 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06048842 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-4d6d6a0d208a45b2ae7e996ab9b18811 |
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| Source note | uspto-grants-2000_04 |
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