(S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

Base Information

Chemical Name:(S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone
CAS No.:130481-72-0
Molecular Formula:C₁₃H₁₁F₃O₇S
Molecular Weight:368.287
Hs Code.:

Synonyms:(S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

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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 (S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

Chemical Property:

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Technology Process of (S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

There total 8 articles about (S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone 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: 96.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 131614-83-0
(2S,4aR,7R,7aR)-7-hydroxy-2-phenyltetrahydro-6H-furo[3,2-d][1,3]dioxin-6-one

: 130481-72-0
(S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

Guidance literature:: With pyridine; In dichloromethane; at -30 - -10 ℃; for 2.25h;
DOI:10.1016/j.tetasy.2004.07.031

Reference yield:

: 87-72-9,608-45-7,608-46-8,608-47-9,2460-44-8,6748-95-4,6763-34-4,7261-26-9,7283-06-9,7283-07-0,7296-55-1,7296-56-2,7296-58-4,7296-59-5,7296-60-8,7296-61-9,7296-62-0,7322-30-7,10257-31-5,10257-32-6,10257-33-7,10257-34-8,10257-35-9,19982-83-3,20242-88-0,28697-53-2,36562-42-2,41546-41-2,89299-64-9,107655-34-5,115794-06-4,115794-07-5,130550-15-1,130606-21-2
D-Xylose

: 130481-72-0
(S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; bromine / H₂O

2: 19.0 g / hydrochloric acid / 20 °C

3: 96 percent / pyridine / CH₂Cl₂ / 2.25 h / -30 - -10 °C

With pyridine; hydrogenchloride; bromine; potassium carbonate; In dichloromethane; water;
DOI:10.1016/j.tetasy.2004.07.031

Reference yield:

: 15384-37-9
D-xylono-1,4-lactone

: 130481-72-0
(S)-3,5-O-benzylidene-2-O-trifluoromethanesulfonyl-D-xylono-1,4-lactone

Guidance literature:: Multi-step reaction with 2 steps

1: 19.0 g / hydrochloric acid / 20 °C

2: 96 percent / pyridine / CH₂Cl₂ / 2.25 h / -30 - -10 °C

With pyridine; hydrogenchloride; In dichloromethane;
DOI:10.1016/j.tetasy.2004.07.031