Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223233Generated: October 26, 2026

Boron trifluoride → 4,4-Dimethyl-6,7-dimethoxy-1-bromomethylisochroman

https://huagongshe.com/reaction/223233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantAcetaldehyde, bromo-HCID 105131—
Reactant2-(3,4-Dimethoxyphenyl)-2-methylpropan-1-olHCID 13015778—
SolventNitromethaneHCID 6375—
Product4,4-Dimethyl-6,7-dimethoxy-1-bromomethylisochromanHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352805
Source datasetuspto-grants-1982_10
ORD IDord-3e4b66a471a743eabefd0a20575541a1
Source noteuspto-grants-1982_10