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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096039Generated: October 29, 2026

Diisopropylamine → HCID 66699464, compound

https://huagongshe.com/reaction/1096039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
Reactant3-Methylthiophene-2-carbonitrileHCID 521617—
Reactant1-(4-Bromo-2-chlorophenyl)ethan-1-oneHCID 15560950—
Reactant4-Bromo-2-chlorobenzeneacetaldehydeHCID 53403616—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66699464HCID 66699464—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyllithium (1.6M) in hexanes (0.18 ml) was added to a solution of diisopropylamine (0.212 ml) in THF (2 ml) at 0° C. The mixture was stirred for 5 min and then cooled to −78° C. 3-Methylthiophene-2-carbonitrile (184 mg, CAS Reg. No. 55406-13-8) was added at −78° C. and then stirred for 30 min. A solution of 2-(4-bromo-2-chlorophenyl)ethanone (248 mg, CAS Reg. No. 749932-89-6, prepared in analogy to Example 58, step 2, from 2-chloro-4-bromoacetophenone [CAS Reg. No. 252561-81-2]) in THF (1 ml) was added at −78° C. The mixture was stirred for 20 min, then water (0.2 ml) was added. The mixture was filtered over celite and concentrated to an oil. The residue was purified by flash chromatography (SiO2, 0 to 100% EtOAc/heptane) to give the title compound (100 mg) as a colorless oil. MS (m/e)=370.0 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138189B2
Source datasetuspto-grants-2012_03
ORD IDord-17615b22984a4cfc84b1a85c614357de
Source noteuspto-grants-2012_03