2(3H)-Furanone, dihydro-5-(4-methoxyphenyl)-, (5S)-

Base Information

Chemical Name:2(3H)-Furanone, dihydro-5-(4-methoxyphenyl)-, (5S)-
CAS No.:128994-28-5
Molecular Formula:C11H12O3
Molecular Weight:192.214
Hs Code.:

Synonyms:

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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, dihydro-5-(4-methoxyphenyl)-, (5S)-

Chemical Property:

Purity/Quality:

Safty Information:

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MSDS Files:: SDS file from LookChem

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Technology Process of 2(3H)-Furanone, dihydro-5-(4-methoxyphenyl)-, (5S)-

There total 30 articles about 2(3H)-Furanone, dihydro-5-(4-methoxyphenyl)-, (5S)- 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: 97.0%

: 1010800-67-5
tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate

: 128994-28-5
(S)-(-)-γ-(p-Methoxyphenyl)-γ-butyrolactone

Guidance literature:: tert-butyl 4-(4-methoxyphenyl)-4-oxobutanoate; With [RuBr₂{(S,S)-2,4-bis-[(3,5-diisopropylphenyl)phosphanyl]pentane}(3-aminomethylisoquinoline)]; potassium tert-butylate; hydrogen; In ethanol; at 25 ℃; for 2h; under 6000.6 Torr; Autoclave;

With potassium tert-butylate; In toluene; at 25 ℃; enantioselective reaction; Inert atmosphere;
DOI:10.1002/anie.201711363

Reference yield: 65.0%

: 4586-89-4
ethyl 4-(4-methoxyphenyl)butanoate

: 128994-28-5
(S)-(-)-γ-(p-Methoxyphenyl)-γ-butyrolactone

Guidance literature:: ethyl 4-(4-methoxyphenyl)butanoate; With ketoreductase-P₂-C₀₂; oxygen; NADPH; 9-(2-mesityl)-10-methylacridinium perchlorate; In water; acetonitrile; at 23 ℃; for 24h; Irradiation; Enzymatic reaction;

With isopropyl alcohol; In water; acetonitrile; enantioselective reaction; Enzymatic reaction;
DOI:10.1002/anie.201909426

Reference yield: 29.0%

: C₁₃H₁₅N₃O₃

: 128994-28-5
(S)-(-)-γ-(p-Methoxyphenyl)-γ-butyrolactone

Guidance literature:: C₁₃H₁₅N₃O₃; With formic acid; N-[(1S,2S)-1,2-diphenyl-2-(3-phenylpropylamino)ethyl]-4-methylbenzene sulfonamide ammonium chloride ruthenium; triethylamine; In water; at 60 ℃; for 24h; Inert atmosphere;

With trifluoroacetic acid; In dichloromethane; water; for 4h; Inert atmosphere;
DOI:10.1021/ol501895k