(R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

Base Information

Chemical Name:(R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol
CAS No.:157189-63-4
Molecular Formula:C₁₇H₂₄O₅S
Molecular Weight:340.441
Hs Code.:

Synonyms:(R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

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Chemical Property of (R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

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Technology Process of (R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

There total 6 articles about (R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-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: 100.0%

: 157189-67-8
1-[(1S,3R,5S,7R)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-one

: 157189-63-4
(R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

Guidance literature:: With L-Selectride; In tetrahydrofuran; at -78 ℃; for 2h;
DOI:10.1248/cpb.42.179

Reference yield:

: 89927-11-7,127757-94-2
7-mesyloxymethyl-3-tosyl-6,8-dioxabicyclo<3.2.1>octane

: 157189-63-4
(R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

Guidance literature:: Multi-step reaction with 6 steps

1: 95 percent / 18-crown-6 / dimethylformamide / 12 h / 80 °C

2: 86 percent / K₂CO₃ / methanol / 12 h / Ambient temperature

3: 85 percent / (COCl)2, DMSO, Et₃N / 5 h / -78 - 0 °C

4: 88 percent / tetrahydrofuran / 1 h / 0 °C

5: 87 percent / Jones reagent / 1 h / 0 °C

6: 100 percent / L-Selectride / tetrahydrofuran / 2 h / -78 °C

With jones reagent; oxalyl dichloride; 18-crown-6 ether; L-Selectride; potassium carbonate; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1248/cpb.42.179

Reference yield:

: [(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-methanol

: 157189-63-4
(R)-1-[(1S,3R,5S,7S)-3-(Toluene-4-sulfonyl)-6,8-dioxa-bicyclo[3.2.1]oct-7-yl]-butan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / (COCl)2, DMSO, Et₃N / 5 h / -78 - 0 °C

2: 88 percent / tetrahydrofuran / 1 h / 0 °C

3: 87 percent / Jones reagent / 1 h / 0 °C

4: 100 percent / L-Selectride / tetrahydrofuran / 2 h / -78 °C

With jones reagent; oxalyl dichloride; L-Selectride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran;
DOI:10.1248/cpb.42.179