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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220681Generated: October 31, 2026

Benzyltrimethylammonium hydroxide → HCID 370270, compound

https://huagongshe.com/reaction/2220681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant1,2-Bis(4-methylphenyl)-1,2-ethanedioneHCID 76996—
Reactant1,3-Bis(4-methylphenyl)propan-2-oneHCID 12420214—
SolventEthanolHCID 702—
ProductHCID 370270HCID 370270—

Reaction Steps

23.13 g (0.11 mol) of 1,3-bis(p-tolyl)-2-propanone and 26.2 g (0.11 mol) of 4,4′-dimethylbenzil were dissolved in 75 ml of hot ethanol (abs.). 53 ml of a methanolic benzyltrimethylammonium hydroxide solution (0.11 mol Triton B, 35% Fluka) were slowly added dropwise at 80° C. with stirring (caution: the reaction batch froths vigorously) and refluxing was effected for 25 minutes. The crude product was filtered off after three hours, then washed with cold ethanol and recrystallized from toluene (violet red, yield: 46.2 g (95%); m.p.: 244-245° C., literature: 250.4-251.4° C. [15]; elemental analysis for C33H38O: found: C, 89.8%, H, 6.6%. calculated: C, 89.96%, H, 6.41%, MS-El [m/z (rel. intensity): M+440 (100), 412 (47), 206 (98), 191 (16), 189 (10)). The IR spectrum of 1,2,3,4-tetra(p-tolyl)cyclopenta-1,3-dien-5-one is shown in FIG. 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417247B2
Source datasetuspto-grants-2008_08
ORD IDord-31efafc87f324f3991366b5227a41a6d
Source noteuspto-grants-2008_08