N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

Base Information

Chemical Name:N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline
CAS No.:159152-09-7
Molecular Formula:C₂₁H₂₁NO₄
Molecular Weight:351.402
Hs Code.:

Synonyms:N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

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Chemical Property of N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

Chemical Property:

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Technology Process of N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

There total 4 articles about N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 75.0%

: 541-41-3
chloroformic acid ethyl ester

: 159152-08-6
1-(α-methylbenzyl)-6,7-methylenedioxy-3,4-dihydroisoquinoline

: 159152-09-7
N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: With potassium carbonate; In chloroform; 0 deg C, 30 min then r.t., 2 h;
DOI:10.1016/S0040-4020(01)89428-X

Reference yield:

: 25145-43-1,36240-11-6,59981-93-0,22414-26-2
2-phenylpropionyl chloride

: 159152-09-7
N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N / CHCl₃ / 2 h / Ambient temperature

2: 98 percent / POCl₃ / acetonitrile / 2 h / Heating

3: 75 percent / K₂CO₃ / CHCl₃ / 0 deg C, 30 min then r.t., 2 h

With potassium carbonate; triethylamine; trichlorophosphate; In chloroform; acetonitrile;
DOI:10.1016/S0040-4020(01)89428-X

Reference yield:

: 1484-85-1
3,4-methylenedioxyphenylethylamine

: 159152-09-7
N-ethoxycarbonyl-1-(α-methylbenzylidene)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / Et₃N / CHCl₃ / 2 h / Ambient temperature

2: 98 percent / POCl₃ / acetonitrile / 2 h / Heating

3: 75 percent / K₂CO₃ / CHCl₃ / 0 deg C, 30 min then r.t., 2 h

With potassium carbonate; triethylamine; trichlorophosphate; In chloroform; acetonitrile;
DOI:10.1016/S0040-4020(01)89428-X