(3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

Base Information

Chemical Name:(3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one
CAS No.:337968-28-2
Molecular Formula:C₂₇H₂₄O₈
Molecular Weight:476.483
Hs Code.:

Synonyms:(3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

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Chemical Property of (3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

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Technology Process of (3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

There total 5 articles about (3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-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: 91.0%

: 120-57-0,30024-74-9
piperonal

: 337968-27-1
(4R,5S)-5-Benzo[1,3]dioxol-5-yl-4-benzyloxymethyl-dihydro-furan-2-one

: 337968-28-2
(3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃;
DOI:10.1055/s-2001-11419

Reference yield:

: 172796-28-0
(R)-4-((benzyloxy)methyl)dihydrofuran-2(3H)-one

: 337968-28-2
(3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / -20 - 0 °C

2: (COCl)2; DMSO; Et₃N / tetrahydrofuran / -78 - -45 °C

3: tetrahydrofuran / 0 °C

4: 69 percent / p-TsOH / benzene / 50 °C

5: 91 percent / LiHMDS / tetrahydrofuran / -78 °C

With oxalyl dichloride; toluene-4-sulfonic acid; dimethyl sulfoxide; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; benzene; 2: Swern oxidation;
DOI:10.1055/s-2001-11419

Reference yield:

: 4-benzyloxy-3-formyl-N,N-dimethyl-butyramide

: 337968-28-2
(3R,4R,5S)-5-Benzo[1,3]dioxol-5-yl-3-(benzo[1,3]dioxol-5-yl-hydroxy-methyl)-4-benzyloxymethyl-dihydro-furan-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 0 °C

2: 69 percent / p-TsOH / benzene / 50 °C

3: 91 percent / LiHMDS / tetrahydrofuran / -78 °C

With toluene-4-sulfonic acid; lithium hexamethyldisilazane; In tetrahydrofuran; benzene;
DOI:10.1055/s-2001-11419