diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

Base Information

Chemical Name:diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate
CAS No.:157831-31-7
Molecular Formula:C₂₇H₃₃NO₉S
Molecular Weight:547.626
Hs Code.:

Synonyms:diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

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Chemical Property of diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

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Technology Process of diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

There total 12 articles about diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate 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: 88.0%

: 124-63-0
methanesulfonyl chloride

: 157831-30-6
diethyl (3R,4R,5S)-2-(3,4-dibenzyloxy-5-hydroxymethylpyrrolidin-2-ylidene)malonate

: 157831-31-7
diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

Guidance literature:: With triethylamine; In dichloromethane;

Reference yield:

: 60933-68-8
3,4,6-tri-O-benzyl-β-D-arabinofuranoside

: 157831-31-7
diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

Guidance literature:: Multi-step reaction with 10 steps

1.1: toluene / 12 h / Heating

2.1: 23.7 g / tetrahydrofuran / 12.5 h / 0 - 20 °C

3.1: 71 percent / PCC; molecular sieves 4 Angstroem / CH₂Cl₂ / 4 h / 20 °C

4.1: O₃/O₂ / ethanol / 0.33 h / -25 °C

4.2: 98 percent / NaBH₄ / ethanol / 0.33 h / 20 °C

5.1: 99 percent / ammonium cerium (IV) nitrate / acetonitrile; H₂O / 1 h / 20 °C

6.1: 89 percent / imidazole / dimethylformamide / 1 h / 20 °C

7.1: 97 percent / Lawesson's reagent / toluene / 0.67 h / 60 °C

8.1: CH₂Cl₂ / 5 h / 20 °C

8.2: 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 3 h

8.3: 82 percent / triphenylphosphine / CH₂Cl₂ / 5 h / 20 °C

9.1: 88 percent / TBAF / tetrahydrofuran / 1.5 h / 20 °C

10.1: 88 percent / Et₃N / CH₂Cl₂ / 2 h / -78 °C

With Lawessons reagent; 1H-imidazole; ammonium cerium(IV) nitrate; 4 A molecular sieve; tetrabutyl ammonium fluoride; oxygen; ozone; triethylamine; pyridinium chlorochromate; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1016/S0040-4020(03)00378-8

Reference yield:

: 157831-27-1
(3S,4R,5S)-3,4-dibenzyloxy-5-hydroxymethyl-1-(4-methoxyphenyl)methyl-pyrrolidin-2-one

: 157831-31-7
diethyl (3R,4R,5S)-2-[3,4-dibenzyloxy-5-(methanesulfonyloxy)methylpyrrolidin-2-ylidene]malonate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 99 percent / ammonium cerium (IV) nitrate / acetonitrile; H₂O / 1 h / 20 °C

2.1: 89 percent / imidazole / dimethylformamide / 1 h / 20 °C

3.1: 97 percent / Lawesson's reagent / toluene / 0.67 h / 60 °C

4.1: CH₂Cl₂ / 5 h / 20 °C

4.2: 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 3 h

4.3: 82 percent / triphenylphosphine / CH₂Cl₂ / 5 h / 20 °C

5.1: 88 percent / TBAF / tetrahydrofuran / 1.5 h / 20 °C

6.1: 88 percent / Et₃N / CH₂Cl₂ / 2 h / -78 °C

With Lawessons reagent; 1H-imidazole; ammonium cerium(IV) nitrate; tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1016/S0040-4020(03)00378-8