(S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

Base Information

Chemical Name:(S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate
CAS No.:1591704-32-3
Molecular Formula:C₁₆H₁₆O₄
Molecular Weight:272.301
Hs Code.:

Synonyms:(S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

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Chemical Property of (S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

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Technology Process of (S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

There total 1 articles about (S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate 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: 73.0%

: 86352-16-1
2-(Furan-2-yl)-2-hydroxy-1-phenylethanone

: 123-20-6,24991-31-9
vinyl n-butyrate

: 86358-28-3
1-(furan-2-yl)-2-phenyl-ethane-1,2-dione

: 1591704-32-3
(S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

: 1591704-38-9
C₁₆H₁₆O₄

Guidance literature:: With [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; lipase TL from Pseudomonas stutzeri; potassium tert-butylate; 1,4-di(diphenylphosphino)-butane; In tetrahydrofuran; at 20 ℃; for 24h; enantioselective reaction; Inert atmosphere; Schlenk technique; Enzymatic reaction;
DOI:10.1021/ol500764q

Reference yield: 90.0%

: 1591704-32-3
(S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

: S-(+)-1-phenyl-2-(2-furyl)-2-hydroxyethanone

Guidance literature:: With lipase TL from Pseudomonas stutzeri; In tetrahydrofuran; aq. phosphate buffer; at 20 ℃; for 16h; pH=7; Inert atmosphere; Enzymatic reaction;
DOI:10.1021/ol500764q

Reference yield:

: 1591704-32-3
(S)-1-(furan-2-yl)-2-phenyl-2-oxoethyl butyrate

: 1591704-34-5
(1R,2S)-1-(furan-2-yl)-2-phenylpent-4-ene-1,2-diol

Guidance literature:: Multi-step reaction with 2 steps

1: lipase TL from Pseudomonas stutzeri / tetrahydrofuran; aq. phosphate buffer / 16 h / 20 °C / pH 7 / Inert atmosphere; Enzymatic reaction

2: indium / tetrahydrofuran; water / 48 h / 40 °C / Inert atmosphere

With indium; lipase TL from Pseudomonas stutzeri; In tetrahydrofuran; aq. phosphate buffer; water;
DOI:10.1021/ol500764q