(2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

Base Information

Chemical Name:(2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine
CAS No.:135304-79-9
Molecular Formula:C₁₉H₂₇ClO₃
Molecular Weight:338.875
Hs Code.:

Synonyms:(2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

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Chemical Property of (2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

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Technology Process of (2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

There total 4 articles about (2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine 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: 45.0%

: 1125-88-8
benzaldehyde dimethyl acetal

: 135304-78-8
(3R,4S)-4-Chloromethyl-3-((S)-1-hydroxy-5-methyl-hexyl)-tetrahydro-furan-2-ol

: 135304-79-9
(2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

Guidance literature:: With toluene-4-sulfonic acid; In dichloromethane; at 0 ℃;
DOI:10.1016/S0040-4039(00)74338-3

Reference yield:

: 109215-47-6
(2R,3R,1'S)-(-)-3-Hydroxymethyl-2-(1'-hydroxy-5'-methylhexyl)-4-butanolide

: 135304-79-9
(2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

Guidance literature:: Multi-step reaction with 3 steps

1: 1) p-bromobenzenesulfonyl chloride, pyridine, 2) KCl, 18-crown-6 / 1) 0 deg C, 2) CH₃CN

2: diisobutylaluminium hydride / toluene / -78 °C

3: 45 percent / TsOH / CH₂Cl₂ / 0 °C

With pyridine; 18-crown-6 ether; potassium chloride; diisobutylaluminium hydride; toluene-4-sulfonic acid; 4-bromobenzenesulfonyl chloride; In dichloromethane; toluene;
DOI:10.1016/S0040-4039(00)74338-3

Reference yield:

: 122922-47-8
(3R,4R)-4-Hydroxymethyl-3-(5-methyl-hexanoyl)-dihydro-furan-2-one

: 135304-79-9
(2S,4S,4aR,5S,7aS)-5-Chloromethyl-4-(4-methyl-pentyl)-2-phenyl-tetrahydro-furo[2,3-d][1,3]dioxine

Guidance literature:: Multi-step reaction with 4 steps

1: NaBH₄ / methanol

2: 1) p-bromobenzenesulfonyl chloride, pyridine, 2) KCl, 18-crown-6 / 1) 0 deg C, 2) CH₃CN

3: diisobutylaluminium hydride / toluene / -78 °C

4: 45 percent / TsOH / CH₂Cl₂ / 0 °C

With pyridine; sodium tetrahydroborate; 18-crown-6 ether; potassium chloride; diisobutylaluminium hydride; toluene-4-sulfonic acid; 4-bromobenzenesulfonyl chloride; In methanol; dichloromethane; toluene;
DOI:10.1016/S0040-4039(00)74338-3