(S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

Base Information

Chemical Name:(S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate
CAS No.:1186240-96-9
Molecular Formula:C₂₄H₃₁NO₆S
Molecular Weight:461.579
Hs Code.:

Synonyms:(S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

Suppliers and Price of (S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

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Chemical Property of (S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

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Technology Process of (S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

There total 4 articles about (S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate 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:

: 874-63-5
3,5-dimethylmethoxybenzene

: 1186240-96-9
(S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

Guidance literature:: Multi-step reaction with 3 steps

1: chlorosulfonic acid / dichloromethane / 0 °C

2: triethylamine / dichloromethane / 0 - 20 °C

3: sodium hydroxide / tetrabutyl-ammonium chloride / water; toluene / 0 - 20 °C

With chlorosulfonic acid; triethylamine; sodium hydroxide; tetrabutyl-ammonium chloride; In dichloromethane; water; toluene;

Reference yield:

: 55661-08-0
4-methoxy-2,6-dimethylbenzenesulfonyl chloride

: 1186240-96-9
(S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: sodium hydroxide / tetrabutyl-ammonium chloride / water; toluene / 0 - 20 °C

With triethylamine; sodium hydroxide; tetrabutyl-ammonium chloride; In dichloromethane; water; toluene;

Reference yield:

: 79815-20-6,78348-24-0
(S)-indoline-2-carboxylic acid

: 1186240-96-9
(S)-tert-butyl 2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)indolin-2-yl)methoxy)acetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: dimethylsulfide borane complex; boron trifluoride diethyl etherate / tetrahydrofuran / Reflux

1.2: Reflux

2.1: triethylamine / dichloromethane / 0 - 20 °C

3.1: sodium hydroxide / tetrabutyl-ammonium chloride / water; toluene / 0 - 20 °C

With dimethylsulfide borane complex; boron trifluoride diethyl etherate; triethylamine; sodium hydroxide; tetrabutyl-ammonium chloride; In tetrahydrofuran; dichloromethane; water; toluene;