(2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Base Information

Chemical Name:(2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester
CAS No.:169774-63-4
Molecular Formula:C₂₀H₂₂F₃NO₈S
Molecular Weight:493.458
Hs Code.:

Synonyms:(2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Suppliers and Price of (2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

There total 6 articles about (2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic 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:

: 40216-83-9
L-4-hydroxyproline methyl ester hydrochloride

: 169774-63-4
(2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / NaHCO₃ / H₂O; tetrahydrofuran / 1.5 h / Ambient temperature

2: 85 percent / RuCl₃*3H₂O, NaIO₄ / acetonitrile; CCl₄; H₂O / 3.5 h / Ambient temperature

3: 100 percent / benzene / 0.33 h / Heating

4: 1.) K₂CO₃, 2.) acetic acid / 1.) acetonitrile, reflux, 18 h, 2.) CHCl₃, H₂O, room temperature, 5.5 h.

5: 1.) LiHMDS, 2.) N,N'-dimethyl-N,N'-propylene urea / 1.) THF, -78 deg C, 40 min, 2.) THF, room temperature, 16 h.

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; ruthenium trichloride; sodium periodate; sodium hydrogencarbonate; potassium carbonate; acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; tetrachloromethane; water; acetonitrile; benzene;
DOI:10.1016/S0040-4020(97)00190-7

Reference yield:

: 31560-20-0,120806-96-4
(2S,4R)-1-benzoyl-4-hydroxypyrrolidine-2-carboxylic acid methyl ester

: 169774-63-4
(2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / RuCl₃*3H₂O, NaIO₄ / acetonitrile; CCl₄; H₂O / 3.5 h / Ambient temperature

2: 100 percent / benzene / 0.33 h / Heating

3: 1.) K₂CO₃, 2.) acetic acid / 1.) acetonitrile, reflux, 18 h, 2.) CHCl₃, H₂O, room temperature, 5.5 h.

4: 1.) LiHMDS, 2.) N,N'-dimethyl-N,N'-propylene urea / 1.) THF, -78 deg C, 40 min, 2.) THF, room temperature, 16 h.

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; ruthenium trichloride; sodium periodate; potassium carbonate; acetic acid; lithium hexamethyldisilazane; In tetrachloromethane; water; acetonitrile; benzene;
DOI:10.1016/S0040-4020(97)00190-7

Reference yield:

: 98-88-4
benzoyl chloride

: 169774-63-4
(2S,3R)-1-Benzoyl-3-tert-butoxycarbonylmethyl-4-trifluoromethanesulfonyloxy-2,3-dihydro-1H-pyrrole-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / NaHCO₃ / H₂O; tetrahydrofuran / 1.5 h / Ambient temperature

2: 85 percent / RuCl₃*3H₂O, NaIO₄ / acetonitrile; CCl₄; H₂O / 3.5 h / Ambient temperature

3: 100 percent / benzene / 0.33 h / Heating

4: 1.) K₂CO₃, 2.) acetic acid / 1.) acetonitrile, reflux, 18 h, 2.) CHCl₃, H₂O, room temperature, 5.5 h.

5: 1.) LiHMDS, 2.) N,N'-dimethyl-N,N'-propylene urea / 1.) THF, -78 deg C, 40 min, 2.) THF, room temperature, 16 h.

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; ruthenium trichloride; sodium periodate; sodium hydrogencarbonate; potassium carbonate; acetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; tetrachloromethane; water; acetonitrile; benzene;
DOI:10.1016/S0040-4020(97)00190-7