(1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

Base Information

Chemical Name:(1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol
CAS No.:144788-28-3
Molecular Formula:C₁₃H₁₆F₂OS
Molecular Weight:258.332
Hs Code.:

Synonyms:(1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

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Chemical Property of (1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

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Technology Process of (1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

There total 5 articles about (1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-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: 95.0%

: 144788-29-4
(1S,3S,5R,R_S)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfinyl>cyclopentan-1-ol

: 144788-28-3
(1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

Guidance literature:: With trifluoroacetic anhydride; sodium iodide; In acetone; at -40 ℃; for 0.166667h;
DOI:10.1016/S0040-4020(01)86600-X

Reference yield:

: 1517-82-4
(-)-menthyl p-toluenesulfinate

: 144788-28-3
(1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 1) Mg, I₂ / 1) ether, 2h, 2) benzene, RT, 30 min

2: 1) LDA / 1) THF, 3 min, 2) THF, -65 deg C, 5 min

3: 13.3 percent / NaBH₄, aq. NH₃ / methanol / 0.17 h / -20 °C

4: 69.9 percent / Bu₃SnH / benzene / 0.07 h / 35 °C / Irradiation

5: 95 percent / NaI, (CF₃CO)2O / acetone / 0.17 h / -40 °C

With ammonium hydroxide; sodium tetrahydroborate; iodine; tri-n-butyl-tin hydride; magnesium; trifluoroacetic anhydride; sodium iodide; lithium diisopropyl amide; In methanol; acetone; benzene;
DOI:10.1016/S0040-4020(01)86600-X

Reference yield:

: 115878-98-3
(R)-1-(but-3-ene-1-sulfinyl)-4-methyl-benzene

: 144788-28-3
(1S,3S,5R)-2,2-difluoro-3-methyl-5-<(4-methylphenyl)sulfenyl>cyclopentan-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 1) LDA / 1) THF, 3 min, 2) THF, -65 deg C, 5 min

2: 13.3 percent / NaBH₄, aq. NH₃ / methanol / 0.17 h / -20 °C

3: 69.9 percent / Bu₃SnH / benzene / 0.07 h / 35 °C / Irradiation

4: 95 percent / NaI, (CF₃CO)2O / acetone / 0.17 h / -40 °C

With ammonium hydroxide; sodium tetrahydroborate; tri-n-butyl-tin hydride; trifluoroacetic anhydride; sodium iodide; lithium diisopropyl amide; In methanol; acetone; benzene;
DOI:10.1016/S0040-4020(01)86600-X