(S,S)-(+)-2-fluorocyclopentanol

Base Information

Chemical Name:(S,S)-(+)-2-fluorocyclopentanol
CAS No.:1214921-47-7
Molecular Formula:C₅H₉FO
Molecular Weight:104.124
Hs Code.:

Synonyms:

Suppliers and Price of (S,S)-(+)-2-fluorocyclopentanol

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of (S,S)-(+)-2-fluorocyclopentanol

Chemical Property:

Purity/Quality:

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Technology Process of (S,S)-(+)-2-fluorocyclopentanol

There total 6 articles about (S,S)-(+)-2-fluorocyclopentanol 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: 79.0%

: 285-67-6,149827-17-8
(1S,5R)-6-Oxa-bicyclo[3.1.0]hexane

: 1214921-47-7
(S,S)-(+)-2-fluorocyclopentanol

Guidance literature:: With 1,1,1,3',3',3'-hexafluoro-propanol; benzoyl fluoride; C₇₂H₉₈Co₂N₄O₈; DBN; In diethyl ether; at 24 ℃; for 18h; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ja207256s

Reference yield: 40.0%

: 108-05-4,9003-20-7
vinyl acetate

: trans-2-fluorocyclopentan-1-ol

: 1214921-47-7
(S,S)-(+)-2-fluorocyclopentanol

: (1R,2R)-2-fluorocyclopentyl acetate

Guidance literature:: With burkholderia cepacia lipase immobilized on diatomite; In tert-butyl methyl ether; at 20 ℃; enantioselective reaction; Inert atmosphere; Enzymatic reaction;
DOI:10.24820/ARK.5550190.P011.634

Reference yield:

: 285-67-6
Cyclopentene oxide

: 1214921-47-7
(S,S)-(+)-2-fluorocyclopentanol

: 1993-91-5,13378-44-4,20421-49-2
(1R,2R)-2-fluorocyclopentan-1-ol

Guidance literature:: Cyclopentene oxide; (R,R)-(-)-(salen)chromium chloride; In acetonitrile; at 20 ℃; for 0.25h;

With silver fluoride; In acetonitrile; at 50 ℃; for 72h; Further stages. Title compound not separated from byproducts.;
DOI:10.1002/1615-4169(200202)344:2<165::AID-ADSC165>3.0.CO;2-1