2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

Base Information

Chemical Name:2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine
CAS No.:82002-68-4
Molecular Formula:C₂₄H₃₆N₂O₄
Molecular Weight:416.561
Hs Code.:

Synonyms:2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

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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 2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

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Technology Process of 2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

There total 1 articles about 2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine 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:

: 64198-57-8
5-(3,4,4-trimethyl-oxazolidin-2-yl)-pyrrolidin-2-one

: 82002-67-3
7-bromoheptyl benzoate

: 82002-68-4
2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

Guidance literature:: With sodium hydride; Yield given. Multistep reaction;
DOI:10.1002/jhet.5570180833

Reference yield: 77.0%

: 82002-68-4
2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

: 82002-69-5
1-<(7-benzoyloxyheptyl)-2-formyl-5-oxo>pyrrolidine

Guidance literature:: With trifluoroacetic acid; In tetrahydrofuran; water; for 4h; Ambient temperature;
DOI:10.1002/jhet.5570180833

Reference yield:

: 82002-68-4
2-<5-oxo-1-(7-benzoyloxyheptyl)-2-pyrrolidinyl>-3,4,4-trimethyloxazolidine

: 82002-70-8
(E)-<1-(7-benzoyloxyheptyl)-2-(3-oxo-2-octenyl)-5-oxo>pyrrolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / CF₃COOH / H₂O; tetrahydrofuran / 4 h / Ambient temperature

2: 1.)n-BuLi / 1.)THF, 0 deg C, 20 min 2.)THF, 0 deg C, 3.5 h

With n-butyllithium; trifluoroacetic acid; In tetrahydrofuran; water;
DOI:10.1002/jhet.5570180833