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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580944Generated: October 27, 2026

Dimethylformamide → 3,3'-Bis(3-Dimethylamino-2-methylpropoxy)Benzil

https://huagongshe.com/reaction/1580944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-Naphthalenesulfonic acidHCID 8420—
Reactant3-Chloro-2-methylpropyl(dimethyl)amineHCID 90906—
Reactant3,3'-Dihydroxybenzil dithallium saltHCID 86733020—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product3,3'-Bis(3-Dimethylamino-2-methylpropoxy)BenzilHCID 21532276—

Reaction Steps

To a dry, stirred suspension of 3,3'-dihydroxybenzil dithallium salt (20 g.) in toluene (250 ml.) and N,N-dimethylformamide (250 ml.) was added dropwise 104 ml. of a solution containing 48 g. of 3-dimethylamino-2-methylpropyl chloride in 500 ml. of toluene. The mixture was stirred and heated under reflux overnight. The resulting heavy white precipitate was removed and washed with toluene. The toluene solution and washings were evaporated to a syrup which was subjected to further evaporation using an oil pump vacuum. The syrup was dissolved in chloroform and applied to a column (48 × 5.2 cm) of a "dry column grade" alumina (Woelm) prepacked in chloroform. Elution was with chloroform and 500 ml. fractions (1 and 2) and 250 ml. (3-6) fractions were collected. Fractions 3-6 were pooled and evaporated to give 10.00 g. of syrup. To 7.55 g. of this material in ethanol (150 ml.) was added naphthalene-2-sulfonic acid (7.72 g.). The solution was warmed and decolorized. Evaporation and addition of seeds and ether gave the title product (9.88 g.) as the bis(2-naphthalenesulfonate) salt; m.p. 162-164°. Recrystallization with decolorization gave pure product; m.p. 164-166°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03935191
Source datasetuspto-grants-1976_01
ORD IDord-89f15f8b1034403888ca0c2cf309d5d7
Source noteuspto-grants-1976_01