(R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

Base Information

Chemical Name:(R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate
CAS No.:1567850-21-8
Molecular Formula:C₂₀H₁₈F₃NO₃S
Molecular Weight:409.429
Hs Code.:

Synonyms:(R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

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Chemical Property of (R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

Chemical Property:

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Technology Process of (R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

There total 12 articles about (R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-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:

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

: 811-68-7
silver(I) trifluoromethanethiolate

: 1567850-19-4
(S)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

: 1567850-21-8
(R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

Guidance literature:: With hydroquinine 1,4-phthalazinediyl diether; trichloroisocyanuric acid; In dichloromethane; at 30 ℃; for 12h; Reagent/catalyst; Solvent; Temperature; enantioselective reaction;
DOI:10.1021/ol5006888

Reference yield:

: 91-56-5,1186480-61-4,84788-92-1
indole-2,3-dione

: 1567850-21-8
(R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0.5 h / -15 °C

1.2: -15 - 20 °C

2.1: tin(ll) chloride; hydrogenchloride / acetic acid / 4 h / Reflux

3.1: ethylmagnesium bromide / tetrahydrofuran; diethyl ether / 4 h / -40 °C

4.1: trichloroisocyanuric acid; hydroquinine 1,4-phthalazinediyl diether / dichloromethane / 12 h / 30 °C

With hydrogenchloride; hydroquinine 1,4-phthalazinediyl diether; trichloroisocyanuric acid; ethylmagnesium bromide; sodium hydride; tin(ll) chloride; In tetrahydrofuran; diethyl ether; dichloromethane; acetic acid;
DOI:10.1021/ol5006888

Reference yield:

: 100-58-3
phenylmagnesium bromide

: 1567850-21-8
(R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran / 0.5 h / -15 °C

1.2: -15 - 20 °C

2.1: tin(ll) chloride; hydrogenchloride / acetic acid / 4 h / Reflux

3.1: ethylmagnesium bromide / tetrahydrofuran; diethyl ether / 4 h / -40 °C

4.1: trichloroisocyanuric acid; hydroquinine 1,4-phthalazinediyl diether / dichloromethane / 12 h / 30 °C

With hydrogenchloride; hydroquinine 1,4-phthalazinediyl diether; trichloroisocyanuric acid; ethylmagnesium bromide; sodium hydride; tin(ll) chloride; In tetrahydrofuran; diethyl ether; dichloromethane; acetic acid;
DOI:10.1021/ol5006888