(-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

Base Information

Chemical Name:(-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate
CAS No.:116142-70-2
Molecular Formula:C₂₂H₂₆O₆S
Molecular Weight:418.511
Hs Code.:

Synonyms:(-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

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Technology Process of (-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

There total 7 articles about (-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate 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: 90.0%

: 120236-99-9
(-)-<(1R,2R,4R)-4-<(benzyloxy)methyl>-2-hydroxycyclopentyl>methyl benzoate

: 124-63-0
methanesulfonyl chloride

: 116142-70-2
(-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

Guidance literature:: With triethylamine; In dichloromethane; for 3h; Ambient temperature;
DOI:10.1021/jm00128a029

Reference yield:

: 120236-98-8
(-)-(1R,2R,4R)-4-<(benzyloxy)methyl>-2-hydroxycyclopentanemethanol

: 116142-70-2
(-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / pyridine / CH₂Cl₂ / 0.17 h

2: 90 percent / Et₃N / CH₂Cl₂ / 3 h / Ambient temperature

With pyridine; triethylamine; In dichloromethane;
DOI:10.1021/jm00128a029

Reference yield:

: 108275-94-1
(-)-(1R,6R,8R)-3-phenyl-2,4-dioxabicyclo<4.3.0>nonane-8-methanol

: 116142-70-2
(-)-(1R,2R,4R)-2-<(benzoyloxy)methyl>-4-<(benzyloxy)methyl>cyclopentyl methanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) KH / 1.) THF, room temperature, 20 min, 2.) 12 h

2: 98 percent / conc. H₂SO₄ / H₂O / 0.17 h / Heating

3: 99 percent / pyridine / CH₂Cl₂ / 0.17 h

4: 90 percent / Et₃N / CH₂Cl₂ / 3 h / Ambient temperature

With pyridine; sulfuric acid; potassium hydride; triethylamine; In dichloromethane; water;
DOI:10.1021/jm00128a029