tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

Base Information

Chemical Name:tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate
CAS No.:1609114-18-2
Molecular Formula:C₂₂H₂₁F₃N₂O₅
Molecular Weight:450.414
Hs Code.:

Synonyms:tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

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Chemical Property of tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

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Technology Process of tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

There total 4 articles about tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-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: 90.0%

: 862906-97-6
tert-butyl 2-oxo-3-phenylindoline-1-carboxylate

: 371-96-0,37468-00-1
(E)-3,3,3-trifluoro-1-nitroprop-1-ene

: 1609114-18-2
tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

Guidance literature:: With 3-(3,5-bis-trifluoromethyl-phenylamino)-4-{[(S)-(6-methoxy-quinolin-4-yl)-((R)-5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methyl]-amino}-cyclobut-3-ene-1,2-dione; In dichloromethane; at 10 ℃; for 3h; Solvent; Temperature; Concentration; Reagent/catalyst; stereoselective reaction; Molecular sieve;
DOI:10.1002/ejoc.201301457

Reference yield:

: 862906-97-6
tert-butyl 2-oxo-3-phenylindoline-1-carboxylate

: 371-96-0,37468-00-1
(E)-3,3,3-trifluoro-1-nitroprop-1-ene

: 1609114-18-2
tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

: tert-butyl (S)-2-oxo-3-phenyl-3-[(2'S)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

Guidance literature:: With C₃₀H₂₉FN₄O₃; In dichloromethane; at 10 ℃; for 3h; Reagent/catalyst; Overall yield = 71 %; stereoselective reaction; Molecular sieve;
DOI:10.1002/ejoc.201301457

Reference yield:

: 862906-97-6
tert-butyl 2-oxo-3-phenylindoline-1-carboxylate

: 371-96-0,37468-00-1
(E)-3,3,3-trifluoro-1-nitroprop-1-ene

: 1609114-18-2
tert-butyl (R)-2-oxo-3-phenyl-3-[(2'R)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

: tert-butyl (S)-2-oxo-3-phenyl-3-[(2'S)-1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

: tert-butyl 2-oxo-3-phenyl-3-[1,1,1-trifluoro-3-nitropropan-2-yl]indoline-1-carboxylate

Guidance literature:: (E)-3,3,3-trifluoro-1-nitroprop-1-ene; With 1-(3,5-Bis-trifluoromethyl-phenyl)-3-[(R)-quinolin-4-yl-((2R,4S,5R)-5-vinyl-1-aza-bicyclo[2.2.2]oct-2-yl)-methyl]-thiourea; In dichloromethane; at 10 ℃; for 0.25h; Sealed tube; Molecular sieve;

tert-butyl 2-oxo-3-phenylindoline-1-carboxylate; In dichloromethane; at 10 ℃; for 3h; Overall yield = 70 %; enantioselective reaction; Sealed tube; Molecular sieve;
DOI:10.1002/ejoc.201301457