2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

Base Information

Chemical Name:2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline
CAS No.:135615-48-4
Molecular Formula:C₂₉H₃₉NO₃
Molecular Weight:449.634
Hs Code.:

Synonyms:2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

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Chemical Property of 2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

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Technology Process of 2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

There total 4 articles about 2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline 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:

: 133372-88-0
C₂₆H₃₄O₄

: 135615-48-4
2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

Guidance literature:: Multi-step reaction with 4 steps

1: KH / 5 h / 150 - 160 °C

2: thionyl chloride

4: thionyl chloride / benzene / 1.5 h

With thionyl chloride; potassium hydride; In benzene;
DOI:10.1021/jo00019a051

Reference yield:

: 135615-58-6
C₂₉H₄₁NO₄

: 135615-48-4
2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

Guidance literature:: With thionyl chloride; In benzene; for 1.5h; Yield given;
DOI:10.1021/jo00019a051

Reference yield:

: C₂₅H₃₁ClO₃

: 135615-48-4
2-<18'-(17'-(Benzyloxy)-19'-methoxy-14',15',16'-trinorsordaric-1'-enyl)>-4,4-dimethyloxazoline

Guidance literature:: Multi-step reaction with 2 steps

2: thionyl chloride / benzene / 1.5 h

With thionyl chloride; In benzene;
DOI:10.1021/jo00019a051