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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511196Generated: October 28, 2026

1-Bromo-4-tert-butylbenzene → HCID 58576748, compound

https://huagongshe.com/reaction/511196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-tert-butylbenzeneHCID 77595—
ReactantBinap, (A+-)-HCID 634876—
ReactantTert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 58576748HCID 5857674834%

Reaction Steps

To 1-bromo-4-tert-butyl-benzene (639 mg; 3.0 mmol), [1,4]diazepane-1-carboxylic acid tert-butyl ester (500 mg; 2.5 mmol), tris-(dibenzylidenacetone)-dipalladium (0) (45 mg; 0.049 mmol), sodium tert-butoxide (360 mg; 3.75 mmol) and (±)-2,2′-bis-diphenylphosphanyl-[1,1′]binaphthalenyl (92 mg; 0.147 mmol) is added toluene (5 mL) and the resulting mixture is irradiated in a mono-mode microwave oven for 2 hours at 100° C. Further tris-(dibenzylidenacetone)-dipalladium (0) (45 mg; 0.049 mmol) and (±)-2,2′-bis-diphenylphosphanyl-[1,1′]binaphthalenyl (92 mg; 0.147 mmol) are added and microwave irradiation at 120° C. is continued for another hour. The reaction mixture is then diluted with ethyl acetate and filtered. The filtrate is concentrated under high vacuum and the obtained residue is purified by column chromatography on silica gel (hexanes/dichloromethane 50:50 v/v to 100) to afford the desired compound (284 mg; 0.85 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096524B2
Source datasetuspto-grants-2015_08
ORD IDord-72cedb0b2a0f4a718ebda23901efab03
Source noteuspto-grants-2015_08