(3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

Base Information

Chemical Name:(3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene
CAS No.:113133-16-7
Molecular Formula:C₂₁H₂₉NO₂
Molecular Weight:327.467
Hs Code.:

Synonyms:(3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

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Technology Process of (3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

There total 4 articles about (3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene 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:

: 14002-52-9
o-phenylbenzoyl chloride

: 113133-16-7
(3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂ / 2 h / -20 °C

2: 1.) sodium hydride / 1.) THF, 0 deg C, 20 min, 2.) 60 deg C, 12 h

3: 1.) K, NH₃, t-BuOH / 1.) THF, -78 deg C, 10 min, 2.) -78 deg C, 45 min

With ammonia; sodium hydride; tert-butyl alcohol; In dichloromethane;
DOI:10.1021/jo00246a012

Reference yield:

: 947-84-2
2-Biphenylcarboxylic acid

: 113133-16-7
(3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine, methanesulfonyl chloride / CH₂Cl₂ / 1 h / -20 °C

2: CH₂Cl₂ / 2 h / -20 °C

3: 1.) sodium hydride / 1.) THF, 0 deg C, 20 min, 2.) 60 deg C, 12 h

4: 1.) K, NH₃, t-BuOH / 1.) THF, -78 deg C, 10 min, 2.) -78 deg C, 45 min

With ammonia; sodium hydride; methanesulfonyl chloride; triethylamine; tert-butyl alcohol; In dichloromethane;
DOI:10.1021/jo00246a012

Reference yield:

: 113133-13-4
1-<<2(S)-(hydroxymethyl)pyrrolidinyl>carbonyl>-2-phenylbenzene

: 113133-16-7
(3S,4S)-3-ethyl-3-<<2(S)-methoxymethyl)pyrrolidinyl>carbonyl>-4-phenylcyclohex-1-ene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) sodium hydride / 1.) THF, 0 deg C, 20 min, 2.) 60 deg C, 12 h

2: 1.) K, NH₃, t-BuOH / 1.) THF, -78 deg C, 10 min, 2.) -78 deg C, 45 min

With ammonia; sodium hydride; tert-butyl alcohol;
DOI:10.1021/jo00246a012