HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride → 4,4-Dimethyl-6,7-dimethoxy-1-bromomethylisochroman
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Acetaldehyde, bromo- | HCID 105131 | — |
| Reactant | 2-(3,4-Dimethoxyphenyl)-2-methylpropan-1-ol | HCID 13015778 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 4,4-Dimethyl-6,7-dimethoxy-1-bromomethylisochroman | HCID 20523070 | — |
Reaction Steps
A 2,2-Dimethyl-2-(3,4-dimethoxyphenyl)ethanol (0.95 g, 0.0045 m) is stirred with 1.07 g (0.0054 m) of the ethyl acetal of bromoacetaldehyde and 0.19 g (0.0014 m) of BF3 .etherate in 25 ml of nitromethane for 15 hours. The mixture is partitioned between methylene chloride and aqueous sodium carbonate. The organic phase is dried over sodium sulfate and concentrated to yield 1.52 g of 4,4-dimethyl-6,7-dimethoxy-1-bromomethylisochroman. The nmr is consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352805 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-3e4b66a471a743eabefd0a20575541a1 |
| Source note | uspto-grants-1982_10 |