(1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

Base Information

Chemical Name:(1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide
CAS No.:1422176-97-3
Molecular Formula:C₁₃H₁₆FNO₃
Molecular Weight:253.273
Hs Code.:

Synonyms:(1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

Suppliers and Price of (1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

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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 (1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

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Technology Process of (1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

There total 2 articles about (1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide 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: 74.0%

: 1355061-74-3
C₁₂H₁₅NO₃

: 1097193-08-2
N-((fluoromethyl)(oxo)(phenyl)-λ⁶-sulfaneylidene)-4-methylbenzenesulfonamide

: 1422176-97-3
(1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

Guidance literature:: With lithium hexamethyldisilazane; In toluene; at -78 - 25 ℃; for 3.33h; Inert atmosphere;

Reference yield: 74.0%

: 1355061-74-3
C₁₂H₁₅NO₃

: 1422176-84-8
(R)-N-tosyl-S-fluoromethyl-S-phenylsulfoximine

: 1422176-97-3
(1S,2S,3S)-2-(3-methoxylphenyl)-3-fluoro-N-methoxy-N-methyl-cyclopropanecarboxamide

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 - 20 ℃; for 3.33333h; optical yield given as %ee; stereoselective reaction; Inert atmosphere;
DOI:10.1002/anie.201202451