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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658035Generated: October 31, 2026

Dimethylamine → HCID 20374134, compound

https://huagongshe.com/reaction/1658035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantLithium amideHCID 24532—
ReactantHCID 21884963HCID 21884963—
Reactant6-tert-Butyl-4-[(dimethylamino)methyl]-2,3-dimethylphenolHCID 22101590—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 20374134HCID 20374134—

Reaction Steps

To 37.6 grams of the compound of Example 1 and 94 grams of di-n-octadecyl phosphite dissolved in 100 ml of dry N,N-dimethylformamide at 55° to 60° was added 2.16 grams of lithium amide and the reaction temperature raised to 106° and kept at 105° to 107° for 11/4 hours, the evolved dimethylamine being swept out of the reaction mixture by a stream of nitrogen. The reaction mixture was dissolved in about one liter of a solvent mixture of toluene, chloroform and benzene containing 6 grams of acetic acid, filtered free of some insoluble by-product. The clear filtrate was washed successively with water, 6N aqueous hydrochloric acid, and water until the wash water was in the pH range of 5 to 6. The solvent solution of the product was dried over anhydrous sodium sulfate. After removing the drying agent by filtration, the clear filtrate was freed of solvent by distillation at reduced pressures yielding a solid residue which afforded the desired compound as white crystals at 91° to 93° after crystallization from isopropanol (Compound 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962377
Source datasetuspto-grants-1976_06
ORD IDord-edc5d2e0fea746469780e4ddc3438a8f
Source noteuspto-grants-1976_06