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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654131Generated: November 2, 2026

Diisopropylamine → 2-Thiophenecarboxaldehyde, 4,5-dichloro-

https://huagongshe.com/reaction/1654131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantThiophene, 2,3-dichloro-HCID 140207—
ReactantMonosodium phosphateHCID 23672064—
ReactantButyllithiumHCID 178418339—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-Thiophenecarboxaldehyde, 4,5-dichloro-HCID 149424—

Reaction Steps

11.1 g of diisopropylamine in 100 ml of tetrahydrofuran were cooled to -60° C., 49 ml of n-butyllithium were added over 10 minutes. The mixture was stirred for 30 minutes and 10 g of 2,3-dichlorothiophene were added at -60° C. The mixture was stirred for 45 minutes and then 6 m1 of dimethylformamide and 10 ml of tetrahydrofuran were added. The mixture was stirred for 1 and a half hours, allowed to return to room temperature, poured into a saturated aqueous sodium dihydrogenphosphate solution and extracted with isopropyl ether. The solvent was evaporated and, after chromatography on silica (eluent: 95/5 hexane/ethyl acetate), 10.16 g of the expected product were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405865
Source datasetuspto-grants-1995_04
ORD IDord-2e9d3e95778b41dd87a9ba5027be5b93
Source noteuspto-grants-1995_04