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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242802Generated: November 1, 2026

Triethylamine → HCID 21939609, compound

https://huagongshe.com/reaction/1242802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-DioxaneHCID 31275—
Reactant1-Bromo-4-(propan-2-yloxy)benzeneHCID 228088—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
SolventEthyl AcetateHCID 8857—
ProductHCID 21939609HCID 2193960947%

Reaction Steps

1-Bromo-4-isopropoxybenzene was combined with dioxane (10.5 mL) and dichloropalladium(dppf) dichloromethane complex (36 mg) under argon. 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane (0.96 mL) was added followed by triethylamine (1.29 mL). The reaction was heated to 90° C. for 23 hours after which, dichloropalladium(dppf) dichloromethane complex (36 mg), 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (0.96 mL) and triethylamine (1.29 mL) was added. Heating was continued for an additional 19 hours after which, it was cooled to room temperature and diluted with ethyl acetate (25 mL). The mixture was washed with water (2×20 mL) and brine (20 mL). The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. Purification of the residue on silica gel (0% to 50% ethyl acetate/hexane over 40 minutes) gave 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isopropoxybenzene (544 mg). Yield=47%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115741B2
Source datasetuspto-grants-2006_10
ORD IDord-f78268def02a409db2fafb5679b810c8
Source noteuspto-grants-2006_10