benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate

Base Information

Chemical Name:benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate
CAS No.:1124311-40-5
Molecular Formula:C₂₇H₃₀N₂O₆S₂
Molecular Weight:542.677
Hs Code.:

Synonyms:benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate

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Chemical Property of benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate

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Technology Process of benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate

There total 2 articles about benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate 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: 59.0%

: 886576-63-2
2,2-dimethylpent-4-enylcarbamic acid benzyl ester

: Et₃NHN(SO₂Ph)2

: 1124311-40-5
benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; palladium(II) trifluoroacetate; N-fluorobis(benzenesulfon)imide; In ethyl acetate; at 20 ℃;
DOI:10.1021/ja9031659

Reference yield: 59.0%

: 886576-63-2
2,2-dimethylpent-4-enylcarbamic acid benzyl ester

: 133745-75-2
N-fluorobis(benzenesulfon)imide

: 1124311-40-5
benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate

Guidance literature:: With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; palladium(II) trifluoroacetate; triethylammonium benzenesulfonimide; In ethyl acetate; at 20 ℃; for 18h; Inert atmosphere;
DOI:10.1021/ol9000087