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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843228Generated: November 2, 2026

Dimethylformamide → N-tert-Butyl-3-(diazenylmethyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamide

https://huagongshe.com/reaction/1843228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-tert-Butyl-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamideHCID 4806824—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN-tert-Butyl-3-(diazenylmethyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamideHCID 86683745—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 117a (100 g, 0.42 mol, 1.0 equiv) in THF (500 mL) was slowly to added n-BuLi (672 mL, 2.5M in THF, 1.68 mol, 4.0 equiv) at −78° C. under argon. The mixture was stirred for 2 h. DMF (306 g, 4.2 mol, 10.0 equiv) was added to the mixture while the temperature was maintained at −78° C. After another 2.0 h, the reaction was quenched with methanol (500 mL) at −78° C. It was stirred for 0.50 h at room temperature. 80% aqueous hydrate hydrazine (131 g, 2.1 mol) was added and the mixture was refluxed at 65° C. overnight. The organic solvent was removed under reduced pressure. The residue was filtered and the yellow solid collected was washed with water. The solid was dried in vacuo to afford crude 117b, which was used in the next step without further purification. MS: [M+H]+ 280.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946213B2
Source datasetuspto-grants-2015_02
ORD IDord-952d45b23bc7497dbfdcac00fc158693
Source noteuspto-grants-2015_02