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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254444Generated: October 25, 2026

Ethylamine → (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methyl-3-hydroxybenzylamine

https://huagongshe.com/reaction/2254444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantPropylamineHCID 7852—
Reactant(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-ethyl-3-hydroxybenzylamineHCID 10445905—
Reactant3-((Methylamino)methyl)phenolHCID 10486905—
Reactant(E)-N-(6,6-Dimethyl-2-hepten-4-ynyl)-N-propyl-3-hydroxybenzylamineHCID 15290087—
Reactant(E)-N-ethyl-N-(6-methoxy-6-methyl-2-hepten-4-ynyl)-3-hydroxybenzylamineHCID 19744624—
Reactant1-Bromo-6-methoxy-6-methylhept-2-en-4-yneHCID 53783202—
ReactantMonomethylamine methanolHCID 57454252—
SolventMethanolHCID 887—
Product(E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-methyl-3-hydroxybenzylamineHCID 19916986—

Reaction Steps

The 3-hydroxybenzylamine derivatives used in Examples 26 to 48, such as (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-ethyl-3-hydroxybenzylamine, (E)-N-(6,6-dimethyl-2-hepten-4-ynyl)-N-propyl-3-hydroxybenzylamine or (E)-N-ethyl-N-(6-methoxy-6-methyl-2-hepten-4-ynyl)-3-hydroxybenzylamine, were obtained by performing the same reaction as in Referential Example 26 except that in place of the starting methylamine-methanol solution, a methanol solution of ethylamine or propylamine was used and as required, 1-bromo-6-methoxy-6-methyl-2-hepten-4-yne was used instead of 1-bromo-6,6-dimethyl-2-hepten-4-yne was used.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234946
Source datasetuspto-grants-1993_08
ORD IDord-fa3c1194eab94af5aeb960275f79a869
Source noteuspto-grants-1993_08