(2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

Base Information

Chemical Name:(2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine
CAS No.:1374023-18-3
Molecular Formula:C₂₀H₃₁NO
Molecular Weight:301.472
Hs Code.:

Synonyms:(2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

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Chemical Property of (2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

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Technology Process of (2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

There total 3 articles about (2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine 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: 91.0%

: 853180-76-4
(2S,4aS,7R,8aR)-2-cyclohexen-1-yl-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

: 106-96-7
propargyl bromide

: 1374023-18-3
(2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

Guidance literature:: With potassium carbonate; In acetonitrile; Reflux;
DOI:10.1002/ejoc.201101462

Reference yield:

: 1192-88-7
1-cyclohexene-1-carboxaldehyde

: 1374023-18-3
(2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 24 h / 20 °C

2: potassium carbonate / acetonitrile / Reflux

With potassium carbonate; In dichloromethane; acetonitrile;
DOI:10.1002/ejoc.201101462

Reference yield:

: 55179-51-6
(-)-aminomenthol

: 1374023-18-3
(2S,4aS,7R,8aR)-N-propargyl-2-(cyclohexen-1-yl)-4,4,7-trimethyloctahydrobenz[e][1,3]oxazine

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 24 h / 20 °C

2: potassium carbonate / acetonitrile / Reflux

With potassium carbonate; In dichloromethane; acetonitrile;
DOI:10.1002/ejoc.201101462