2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI)

Base Information

Chemical Name:2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI)
CAS No.:169396-08-1
Molecular Formula:C₁₀H₁₈O₅
Molecular Weight:218.25
Hs Code.:
Mol file:169396-08-1.mol

Synonyms:2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI)

Suppliers and Price of 2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI)

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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 2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI)

Chemical Property:

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Technology Process of 2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI)

There total 2 articles about 2(3H)-Furanone,5-butyl-5-ethoxydihydro-3,4-dihydroxy-,[3R-(3alpha,4alpha,5bta)]-(9CI) 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: 66.0%

: 169395-92-0
(S)-5-Butyl-5-ethoxy-5H-furan-2-one

: 169396-07-0,169396-08-1
(3S,4R,5S)-5-Butyl-5-ethoxy-3,4-dihydroxy-dihydro-furan-2-one

Guidance literature:: With perhydrodibenzo-18-crown-6; potassium permanganate; In dichloromethane; 1.) -40 deg C, 4 h, 2.) 0 deg C, 3 h;
DOI:10.1021/jo00117a034

Reference yield:

: 169395-92-0
(S)-5-Butyl-5-ethoxy-5H-furan-2-one

: 169396-07-0,169396-08-1
(3S,4R,5S)-5-Butyl-5-ethoxy-3,4-dihydroxy-dihydro-furan-2-one

: (3R,4S,5S)-5-Butyl-5-ethoxy-3,4-dihydroxy-dihydro-furan-2-one

Guidance literature:: With ruthenium trichloride; sodium periodate; In ethyl acetate; acetonitrile; at 0 ℃; for 0.05h; Yield given. Yields of byproduct given. Title compound not separated from byproducts;
DOI:10.1021/jo00117a034