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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981828Generated: October 30, 2026

Dimethylformamide → HCID 20071127, compound

https://huagongshe.com/reaction/981828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-Bromo-2-chloroanisoleHCID 2769567—
ReactantSilane, [(3,4-dihydro-2-naphthalenyl)oxy]trimethyl-HCID 11042217—
SolventWaterHCID 962—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 20071127HCID 20071127—

Reaction Conditions

Temperature90 °C

Reaction Steps

Charge an oven dried, argon flushed 25-mL 2-necked round bottomed flask equipped with a stirring bar and reflux condenser with 2-trimethylsilyloxy-3,4-dihydronaphthalene (0.4247 grams, 1.9449 mmoles) and tetra-n-butylammonium fluoride (2.3 mL, 2.30 mmoles, 1 M in tetrahydrofuran), stir for a few minutes and then add 4-bromo-2-methoxy-1-chlorobenzene (0.4336 grams, 1.9577 mmoles) dichlorobis(tri-ο-tolyl-phosphine)palladium (0.0154 grams, 0.0196 mmoles) and 5 mL dimethylformamide. Heat the reaction mixture for 18 hours (oil bath temperature about 90° C.), cool to RT and add 5 mL water and 10 mL t-butylmethyl ether. Separate the layers, extract the aqueous layers with 3×5 mL t-butylmethyl ether, wash the combined organic layers with water and saturated salt solution, dry over magnesium sulfate and concentrate using a Buchi rotavapor to yield the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04992591
Source datasetuspto-grants-1991_02
ORD IDord-efd9e7c9dc0741e8a9157ed9e13ac00a
Source noteuspto-grants-1991_02