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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218626Generated: November 1, 2026

5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene → N-[3-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-4-methyl-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/2218626

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cyclohepteneHCID 5257940—
ReactantN-(4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanesulfonamideHCID 59770368—
ProductN-[3-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-4-methyl-phenyl]-methanesulfonamideHCID 5977008361%

Reaction Steps

Following the procedures essentially as described in Example 219, below, and using N-[4-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanesulfonamide (120 mg, 0.386 mmol) and 5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene (100 mg, 0.351 mmol) affords 83 mg (61%) of the title compound as a yellow solid. MS (ES) 407 (M+NH4), 388 (M−H); HPLC shows 91% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411072B2
Source datasetuspto-grants-2008_08
ORD IDord-d3c6ef09856d4ef7ad43add0dac71fcf
Source noteuspto-grants-2008_08