acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester
CAS No.:917814-35-8
Molecular Formula:C₂₈H₃₆O₅
Molecular Weight:452.591
Hs Code.:

Synonyms:acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

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Chemical Property of acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

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Technology Process of acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

There total 5 articles about acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-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: 77.0%

: 884004-61-9
(2R,3S,4R,6S)-2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-ol

: 108-24-7
acetic anhydride

: 917814-35-8
acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

Guidance literature:: With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 48h;
DOI:10.1002/chem.200500993

Reference yield:

: C₁₆H₂₀O₃

: 917814-35-8
acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1: NaBH₄; CeCl₃*7H₂O / methanol / 0 °C

2: 1.28 g / NaH; Bu₄NI / tetrahydrofuran / 12.5 h / 0 - 20 °C

3: dimethyldioxirane / CH₂Cl₂; acetone / 0.3 h / -60 - 20 °C

4: 0.386 g / tetrahydrofuran / 0.3 h / 0 - 20 °C

5: 77 percent / (i-Pr)2NEt; DMAP / CH₂Cl₂ / 48 h / 20 °C

With dmap; sodium tetrahydroborate; cerium(III) chloride; 3,3-dimethyldioxirane; tetra-(n-butyl)ammonium iodide; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; acetone; 1: Luche reduction;
DOI:10.1002/chem.200500993

Reference yield:

: C₂₃H₂₈O₄

: 917814-35-8
acetic acid 2-allyl-4-benzyloxy-6-(3-benzyloxy-propyl)-3-methyl-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 0.386 g / tetrahydrofuran / 0.3 h / 0 - 20 °C

2: 77 percent / (i-Pr)2NEt; DMAP / CH₂Cl₂ / 48 h / 20 °C

With dmap; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1002/chem.200500993