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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018179Generated: November 2, 2026

Formaldehyde → 4,4'-Bis(ethylmethylamino)benzophenone

https://huagongshe.com/reaction/1018179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPhosgeneHCID 6371—
ReactantN-EthylanilineHCID 7670—
ReactantN-Ethyl-N-methylanilineHCID 11956—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product4,4'-Bis(ethylmethylamino)benzophenoneHCID 10935343—

Reaction Conditions

Temperature55 °C

Reaction Steps

Ethyl-aniline is methylated by reductive alkylation with formaldehyde using isopropyl alcohol as a solvent at 100° C. under 120 psi of H2. After the solvent is stripped the product ethylmethylaniline (NEMA) is purified by distillation at 120° C. at a pressure of 21 mm mercury (Hg). NEMA (80 g, 0.59 mol) is charged to a vessel fitted with a dry-ice condenser and is heated to 50-60° C. Phosgene is transferred from a cylinder to a calibrated trap placed in dry-ice. After condensing 10 mL (14.3 g, 0.145 mol), the trap was connected to the vessel containing NEMA and the phosgene was added over 1 hour. After the addition was complete, the mixture was heated to 120° C. and held at this temperature for 1 hour. The mixture was cooled to 50-60° C. before 11 g (0.275 mol) of NaOH dissolved in 100 mL of water was added to hydrolyze the unreacted acid chloride. The resulting mixture was then extracted with two 100 mL portions of toluene. The product 4,4′-bis(methylethylamino)benzophenone (MEAB) was purified by chromatography on silica gel using toluene as an eluent followed by recrystallization from methylene chloride/hexane. Several grams of highly pure MEAB were obtained. No impurities were detectable by NMR; m.p. 122-124° C. NMR, IR and mass spectra were consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479706B1
Source datasetuspto-grants-2002_11
ORD IDord-5642d8c464714fa7afcbf197d44e0e74
Source noteuspto-grants-2002_11