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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53239Generated: October 28, 2026

Dimethylformamide → HCID 11447610, compound

https://huagongshe.com/reaction/53239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-Bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furanHCID 10779312—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11447610HCID 1144761028.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

t-Butyllithium (11.9 mL, 20.3 mmol, 1.7M in pentane) is added dropwise to a solution of 5-bromo-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furan (3.60 g, 12.7 mmol) in 50 mL of anhydrous THF at -78° C.; the resulting reaction mixture is stirred at -78° C. for 15 min and N,N-dimethylformamide (1.0 mL, 13.0 mmol) is introduced. The reaction mixture is kept at -78° C. for 0.5 h, quenched with water, warmed to room temperature, and extracted with ether. The extract is washed with water, dried over anhydrous magnesium sulfate, and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (10%→20% ether-hexane) gives 0.83 g (28%) of 7-tert-butyl-2,3-dihydro-3,3-dimethyl-5-formylbenzo[b]furan as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618835
Source datasetuspto-grants-1997_04
ORD IDord-8382aa719f13415ba067e4a9a410d282
Source noteuspto-grants-1997_04