(2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

Base Information

Chemical Name:(2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester
CAS No.:174874-87-4
Molecular Formula:C₁₉H₂₃NO₇
Molecular Weight:377.394
Hs Code.:

Synonyms:(2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

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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 (2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

There total 4 articles about (2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester 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: 95.0%

: 62269-44-7
methyl 3-trimethylsiloxybut-2-enoate

: 174874-84-1
acetic acid (2S,3S)-2-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-3-yl ester

: 174874-87-4
(2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; 1.) -78 deg C, 1 h, 2.) RT, 1h;
DOI:10.1016/0040-4020(95)01085-8

Reference yield:

: 174874-82-9
acetic acid (3S)-1-(4-methoxy-benzyl)-2,5-dioxo-pyrrolidin-3-yl ester

: 174874-87-4
(2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / NaBH₄ / ethanol; tetrahydrofuran / 0.33 h / -30 °C

2: 100 percent / pyridine, DMAP / 18 h / Ambient temperature

3: 95 percent / TMSOTf / CH₂Cl₂ / 1.) -78 deg C, 1 h, 2.) RT, 1h

With pyridine; dmap; sodium tetrahydroborate; trimethylsilyl trifluoromethanesulfonate; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/0040-4020(95)01085-8

Reference yield:

: 174875-15-1
acetic acid (2S,3S)-2-hydroxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-3-yl ester

: 174874-87-4
(2R,3S)-2-<3-acetoxy-1-(4-methoxy-benzyl)-5-oxo-pyrrolidin-2-yl>-3-oxo-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / pyridine, DMAP / 18 h / Ambient temperature

2: 95 percent / TMSOTf / CH₂Cl₂ / 1.) -78 deg C, 1 h, 2.) RT, 1h

With pyridine; dmap; trimethylsilyl trifluoromethanesulfonate; In dichloromethane;
DOI:10.1016/0040-4020(95)01085-8