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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223645Generated: October 25, 2026

Benzylamine → 3-Ethyl-3-n-butyl-12-phenyl-1-aza-1,5,9-cyclododecatriene

https://huagongshe.com/reaction/223645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant2-Ethylhex-2-EnalHCID 12582—
ReactantN-benzylidene-(2-ethyl-1-hexenylamine)HCID 56636874—
Product3-Ethyl-3-n-butyl-12-phenyl-1-aza-1,5,9-cyclododecatrieneHCID 54523241—

Reaction Steps

The procedure described in Example 1(a) is repeated, except that 215.3 g (1 mol) of N-benzylidene-(2-ethyl-1-hexenylamine) [1-phenyl-4-ethyl-4-n-butyl-2-aza-1,3-butadiene; prepared by reacting benzylamine with 2-ethyl-hexenal and then isomerising the reaction product with potassium tert.-butylate; boiling point 90° C./7 Pa; nD20 =1.5630] are used. Distillation yields 288 g (0.891 mol) of 3-n-butyl-3-ethyl-12-phenyl-1-aza-1,5,9-cyclododecatriene; boiling point 130° C./2 Pa; nD20 =1.5296.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355177
Source datasetuspto-grants-1982_10
ORD IDord-099217fb9a2d4c969136b0514f5ca373
Source noteuspto-grants-1982_10