2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol

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Chemical Name:2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol
CAS No.:848850-76-0
Molecular Formula:C₂₈H₃₅N₂O₄P
Molecular Weight:494.571
Hs Code.:

Synonyms:2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol

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Chemical Property of 2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol

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Technology Process of 2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol

There total 3 articles about 2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol 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: 61.0%

: 848850-67-9
(R)-3-Bromo-1-[2-(diphenyl-phosphinoyl)-6-methoxy-phenyl]-piperidine

: 111-42-2
2,2'-iminobis[ethanol]

: 2-[{(R)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-piperidin-3-yl}-(2-hydroxy-ethyl)-amino]-ethanol

: 848850-76-0
2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol

Guidance literature:: With potassium carbonate; In acetonitrile; for 6h; Heating;
DOI:10.1021/jo0479967

Reference yield:

: 511553-39-2
(S)-1-[2'-(diphenylphosphinyl)-6'-methoxyphenyl]-2-(hydroxymethyl)pyrrolidine

: 848850-76-0
2-[{(S)-1-[2-(Diphenyl-phosphinoyl)-6-methoxy-phenyl]-pyrrolidin-2-ylmethyl}-(2-hydroxy-ethyl)-amino]-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / CBr₄; triphenylphosphine / acetonitrile / 3 h / 20 °C

2: 61 percent / K₂CO₃ / acetonitrile / 6 h / Heating

With carbon tetrabromide; potassium carbonate; triphenylphosphine; In acetonitrile;
DOI:10.1021/jo0479967