Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

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Chemical Name:Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester
CAS No.:118893-67-7
Molecular Formula:C₂₈H₃₆O₅Si
Molecular Weight:480.676
Hs Code.:

Synonyms:Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

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Chemical Property of Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

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Technology Process of Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

There total 4 articles about Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester 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: 86.8%

: 69739-34-0
t-butyldimethylsiyl triflate

: 118893-66-6
Benzoic acid (2R,3R,4R)-2-((E)-3-benzyloxy-propenyl)-4-hydroxy-3,4-dihydro-2H-pyran-3-yl ester

: 118893-67-7
Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; at -78 ℃; for 0.5h;
DOI:10.1021/ja00188a038

Reference yield:

: 87461-94-7
1-methoxy-3-((tert-butyldimethylsilyl)oxy)-4-(benzoyloxy)-1,3-butadiene

: 118893-67-7
Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) BF₃*OEt₂, 2.) trifluoroacetic acid / 1.) dichloromethane, -78 deg C, 5.5 h, 2.) carbon tetrachloride

2: 86 percent / CeCl₃*7H₂O, sodium borohydride / ethanol; methanol / 1 h / -78 °C

3: 86.8 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / -78 °C

With 2,6-dimethylpyridine; sodium tetrahydroborate; cerium(III) chloride; boron trifluoride diethyl etherate; trifluoroacetic acid; In methanol; ethanol; dichloromethane;
DOI:10.1021/ja00188a038

Reference yield:

: 69152-87-0
4-benzyloxycrotonaldehyde

: 118893-67-7
Benzoic acid (R)-2-((E)-3-benzyloxy-propenyl)-4-(tert-butyl-dimethyl-silanyloxy)-3,4-dihydro-2H-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) BF₃*OEt₂, 2.) trifluoroacetic acid / 1.) dichloromethane, -78 deg C, 5.5 h, 2.) carbon tetrachloride

2: 86 percent / CeCl₃*7H₂O, sodium borohydride / ethanol; methanol / 1 h / -78 °C

3: 86.8 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / -78 °C

With 2,6-dimethylpyridine; sodium tetrahydroborate; cerium(III) chloride; boron trifluoride diethyl etherate; trifluoroacetic acid; In methanol; ethanol; dichloromethane;
DOI:10.1021/ja00188a038