Pyrrolidine, 1-(2-fluoro-3-methyl-1-oxo-4-pentenyl)-2,5-dimethyl-, [2R-[1(2S,3S),2alpha,5beta]]- (9CI)

Base Information

Chemical Name:Pyrrolidine, 1-(2-fluoro-3-methyl-1-oxo-4-pentenyl)-2,5-dimethyl-, [2R-[1(2S*,3S*),2alpha,5beta]]- (9CI)
CAS No.:136734-67-3
Molecular Formula:C12H20FNO
Molecular Weight:213.2917032
Hs Code.:
Mol file:136734-67-3.mol

Synonyms:Pyrrolidine, 1-(2-fluoro-3-methyl-1-oxo-4-pentenyl)-2,5-dimethyl-, [2R-[1(2S*,3S*),2alpha,5beta]]- (9CI)

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Chemical Property of Pyrrolidine, 1-(2-fluoro-3-methyl-1-oxo-4-pentenyl)-2,5-dimethyl-, [2R-[1(2S*,3S*),2alpha,5beta]]- (9CI)

Chemical Property:

PSA：20.31000
LogP:2.48390

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Pyrrolidine, 1-(2-fluoro-3-methyl-1-oxo-4-pentenyl)-2,5-dimethyl-, [2R-[1(2S*,3S*),2alpha,5beta]]- (9CI)

There total 3 articles about Pyrrolidine, 1-(2-fluoro-3-methyl-1-oxo-4-pentenyl)-2,5-dimethyl-, [2R-[1(2S*,3S*),2alpha,5beta]]- (9CI) 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:

: 84987-70-2
(E)-2-buten-1-ol lithium salt

: Trifluoro-methanesulfonate(2R,5R)-1-(2-fluoro-1-methoxy-ethylidene)-2,5-dimethyl-pyrrolidinium;

: 136634-12-3
(2R,3R)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

: 136734-68-4
(2R,3S)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

: 136734-66-2
(2S,3R)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

: 136734-67-3
(2S,3S)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

Guidance literature:: In dichloromethane; for 24h; Title compound not separated from byproducts; Ambient temperature;
DOI:10.1016/S0040-4039(00)92145-2

Reference yield:

: 136634-11-2
N-fluoroacetyl-trans-(2R,5R)-2,5-dimethylpyrrolidine

: 84987-70-2
(E)-2-buten-1-ol lithium salt

: 333-27-7
methyl trifluoromethanesulfonate

: 136634-12-3
(2R,3R)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

: 136734-68-4
(2R,3S)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

: 136734-66-2
(2S,3R)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

: 136734-67-3
(2S,3S)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

Guidance literature:: multistep reaction;
DOI:10.1016/S0040-4039(00)92145-2

Reference yield:

: 136634-11-2
N-fluoroacetyl-trans-(2R,5R)-2,5-dimethylpyrrolidine

: 136734-67-3
(2S,3S)-1-((2R,5R)-2,5-Dimethyl-pyrrolidin-1-yl)-2-fluoro-3-methyl-pent-4-en-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 0.5 h / Ambient temperature

2: CH₂Cl₂ / 24 h / Ambient temperature

In dichloromethane;
DOI:10.1016/S0040-4039(00)92145-2