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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198388Generated: November 1, 2026

Dimethylformamide → HCID 19102630, compound

https://huagongshe.com/reaction/1198388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantHCID 19102632HCID 19102632—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19102630HCID 1910263096%

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyllithium (18.6 ml of a 2.5M solution in hexane, 46.5 mmol) and N,N,N',N'-tetramethylethylenediamine (5.38 g, 46.3 mmol), respectively, were added (using a syringe) to a stirred solution of 5-(1-ethoxyethoxy)-1,3-benzodioxole (8.9 g, 42.4 mmol) in dry THF (100 ml) in a nitrogen atmosphere at -78° C. The resulting solution was allowed to attain room temperature and then cooled to -78° C. A solution of N,N-dimethylformamide (3.70 g, 50.6 mmol) in dry THF (20 ml) was added using a syringe, and the reaction mixture was allowed to attain room temperature. The resulting mixture was quenched with water and extracted with diethyl ether (3times). The combined ether layers were washed with water (2 times), dried over Na2SO4, filtered and evaporated in vacuo to to yield 5-(1-ethoxyethoxy)-4-formyl-1,3-benzodioxole (9.7 g, 96% yield; compound No. 2) as a pale yellow solid, m.p. 48°- 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281595
Source datasetuspto-grants-1994_01
ORD IDord-1a1aa75267c34654bd72a6772479a5de
Source noteuspto-grants-1994_01