(1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

Base Information

Chemical Name:(1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol
CAS No.:85576-75-6
Molecular Formula:C₂₁H₃₅NO₄S₂
Molecular Weight:429.645
Hs Code.:

Synonyms:(1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

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Chemical Property of (1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

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Technology Process of (1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

There total 7 articles about (1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol 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: 92.0%

: 85576-71-2
(2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-hexanal

: 61764-06-5
2-lithio-4,5-dihydro-5-methyl-1,3,5-dithiazine

: 85576-75-6
(1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

Guidance literature:: In tetrahydrofuran; at -100 - 0 ℃;
DOI:10.1016/S0040-4039(00)85555-0

Reference yield:

: 7586-22-3,71372-08-2,82917-27-9,85646-66-8,92999-34-3,96612-17-8,100227-53-0,100227-54-1,114884-21-8
methyl hydrogen meso-2,4-dimethylethylglutarate

: 85576-75-6
(1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

Guidance literature:: Multi-step reaction with 7 steps

1: 95 percent / oxalyl chloride / benzene

3: HBF₄

4: methanol

5: LiAlH₄

6: CrO₃*2pyr

7: 92 percent / tetrahydrofuran / -100 - 0 °C

With lithium aluminium tetrahydride; oxalyl dichloride; dipyridine chromium trioxide; tetrafluoroboric acid; In tetrahydrofuran; methanol; benzene;
DOI:10.1016/S0040-4039(00)85555-0

Reference yield:

: 10348-69-3,82924-00-3,85576-66-5,92927-35-0,95273-50-0,102849-16-1
methyl (2R*,4S*)-4-chloromethanoyl 2-methylpentanoate

: 85576-75-6
(1R,2S,4R)-6-Benzyloxy-5,5-dimethoxy-2,4-dimethyl-1-(5-methyl-[1,3,5]dithiazinan-2-yl)-hexan-1-ol

Guidance literature:: Multi-step reaction with 6 steps

2: HBF₄

3: methanol

4: LiAlH₄

5: CrO₃*2pyr

6: 92 percent / tetrahydrofuran / -100 - 0 °C

With lithium aluminium tetrahydride; dipyridine chromium trioxide; tetrafluoroboric acid; In tetrahydrofuran; methanol;
DOI:10.1016/S0040-4039(00)85555-0