(R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

Base Information

Chemical Name:(R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol
CAS No.:1370293-20-1
Molecular Formula:C₂₂H₂₈ClNO₅S
Molecular Weight:453.987
Hs Code.:

Synonyms:(R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

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Chemical Property of (R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

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Technology Process of (R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

There total 3 articles about (R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol 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: 88.0%

: 1633-82-5
3-chloro-n-propanesulfonyl chloride

: 1237893-91-2
(R)-bis(3-methoxyphenyl)(pyrrolidin-2-yl)methanol

: 1370293-20-1
(R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 2h;
DOI:10.1021/jm201627n

Reference yield:

: 1370292-93-5
(R)-ethyl 2-(hydroxybis(3-methoxyphenyl)methyl)pyrrolidine-1-carboxylate

: 1370293-20-1
(R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; potassium hydroxide / 12 h / Reflux

2: triethylamine / dichloromethane / 2 h / 0 - 20 °C

With methanol; triethylamine; potassium hydroxide; In dichloromethane;
DOI:10.1021/jm201627n

Reference yield:

: 36282-40-3
(3-methoxyphenyl)magnesium bromide

: 1370293-20-1
(R)-(1-(3-chloropropylsulfonyl)pyrrolidin-2-yl)bis(3-methoxyphenyl)methanol

Guidance literature:: Multi-step reaction with 3 steps

1: tetrahydrofuran / 3 h / 0 °C

2: methanol; potassium hydroxide / 12 h / Reflux

3: triethylamine / dichloromethane / 2 h / 0 - 20 °C

With methanol; triethylamine; potassium hydroxide; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm201627n