2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

Base Information

Chemical Name:2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide
CAS No.:438627-78-2
Molecular Formula:C₂₀H₂₇NO₅
Molecular Weight:361.438
Hs Code.:

2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3a<i>H</i>-cyclopenta[1,3]dioxol-4-yl]-<i>N</i>,<i>N</i>-dimethyl-acetamide

Synonyms:2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

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Chemical Property of 2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

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Technology Process of 2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

There total 7 articles about 2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide 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: 76.0%

: 18871-66-4
N,N-dimethylacetamide dimethyl acetal

: 438627-77-1
(3aS,4S,6aR)-6-(3,4-Dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-ol

: 438627-78-2
2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

Guidance literature:: In decalin; at 220 ℃;
DOI:10.1016/S0040-4039(02)00033-3

Reference yield:

: 2859-78-1
4-Bromoveratrole

: 438627-78-2
2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / butyllithium / tetrahydrofuran / -78 °C

2: 94 percent / tetrabutylammonium fluoride / tetrahydrofuran

3: pyridinium chlorochromate; NaOAc

4: acetic acid / 40 °C

5: 98 percent / NaBH₄; CeCl₃*7H₂O / methanol / -20 °C

6: 76 percent / decahydronaphthalene / 220 °C

With sodium tetrahydroborate; n-butyllithium; cerium(III) chloride; tetrabutyl ammonium fluoride; sodium acetate; pyridinium chlorochromate; In tetrahydrofuran; methanol; acetic acid; decalin; 6: Eschenmoser reaction;
DOI:10.1016/S0040-4039(02)00033-3

Reference yield:

: 288269-05-6
(3aS,6R,6aR)-6-(tert-Butyl-dimethyl-silanyloxy)-2,2-dimethyl-tetrahydro-cyclopenta[1,3]dioxol-4-one

: 438627-78-2
2-[4-(3,4-dimethoxy-phenyl)-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[1,3]dioxol-4-yl]-N,N-dimethyl-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 80 percent / butyllithium / tetrahydrofuran / -78 °C

2: 94 percent / tetrabutylammonium fluoride / tetrahydrofuran

3: pyridinium chlorochromate; NaOAc

4: acetic acid / 40 °C

5: 98 percent / NaBH₄; CeCl₃*7H₂O / methanol / -20 °C

6: 76 percent / decahydronaphthalene / 220 °C

With sodium tetrahydroborate; n-butyllithium; cerium(III) chloride; tetrabutyl ammonium fluoride; sodium acetate; pyridinium chlorochromate; In tetrahydrofuran; methanol; acetic acid; decalin; 6: Eschenmoser reaction;
DOI:10.1016/S0040-4039(02)00033-3