1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one

Base Information

Chemical Name:1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one
CAS No.:1168107-60-5
Molecular Formula:C₁₈H₂₂O₆
Molecular Weight:334.369
Hs Code.:

Synonyms:1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one

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Chemical Property of 1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one

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Technology Process of 1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one

There total 1 articles about 1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one 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: 95.0%

: 1192322-83-0
C₁₈H₂₄O₆

: 1168107-60-5
1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one

Guidance literature:: With Dess-Martin periodane; In dichloromethane; for 1h; Inert atmosphere;
DOI:10.1016/j.tet.2010.09.084

Reference yield: 92.0%

: 1168107-60-5
1-((3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-tetrahydro-2,2-dimethylfuro[2,3-d][1,3]dioxol-5-yl)prop-2-en-1-one

: 542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene

: 1168107-61-6
((1S,2S,4S)-bicyclo[2.2.1]hept-5-en-2-yl(3aR,5S,6R,6aR)-6-(4-methoxybenzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanone

Guidance literature:: With zinc(II) chloride; In dichloromethane; at -78 ℃; for 5h; diastereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2010.09.084