{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester
CAS No.:791838-49-8
Molecular Formula:C₂₇H₃₄N₂O₃
Molecular Weight:434.579
Hs Code.:

{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

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Chemical Property of {1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

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Technology Process of {1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

There total 9 articles about {1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester 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: 90.0%

: 122536-76-9,140629-77-2
3(S)-(tert-butoxycarbonylamino)pyrrolidine

: 791838-48-7
trifluoro-methanesulfonic acid 2-(4-phenyl-butyl)-benzofuran-4-yl ester

: 791838-49-8
{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: With palladium diacetate; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; In toluene; Heating;
DOI:10.1016/j.bmcl.2004.07.055

Reference yield:

: 7484-37-9
(3-phenylpropyl)triphenylphosphonium bromide

: 791838-49-8
{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 85 percent / n-BuLi / tetrahydrofuran / 0 - 25 °C

2: 99 percent / H₂ / Pd/C / ethyl acetate

3: 96 percent / LiAlH₄ / tetrahydrofuran / 20 °C

4: 90 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂

5: MCPBA / CHCl₃

6: HCl / methanol

7: pyridine / 0 - 25 °C

8: 90 percent / Pd(OAc)2; BINAP; Cs₂CO₃ / toluene / Heating

With pyridine; hydrogenchloride; palladium diacetate; lithium aluminium tetrahydride; n-butyllithium; oxalyl dichloride; hydrogen; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; ethyl acetate; toluene; 1: Wittig olefination / 4: Swern oxidation / 5: Baeyer-Villiger oxidation;
DOI:10.1016/j.bmcl.2004.07.055

Reference yield:

: 532399-76-1
ethyl 2-Formylbenzo[b]furan-4-carboxylate

: 791838-49-8
{1-[2-(4-phenyl-butyl)-benzofuran-4-yl]-pyrrolidin-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 85 percent / n-BuLi / tetrahydrofuran / 0 - 25 °C

2: 99 percent / H₂ / Pd/C / ethyl acetate

3: 96 percent / LiAlH₄ / tetrahydrofuran / 20 °C

4: 90 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂

5: MCPBA / CHCl₃

6: HCl / methanol

7: pyridine / 0 - 25 °C

8: 90 percent / Pd(OAc)2; BINAP; Cs₂CO₃ / toluene / Heating

With pyridine; hydrogenchloride; palladium diacetate; lithium aluminium tetrahydride; n-butyllithium; oxalyl dichloride; hydrogen; caesium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; chloroform; ethyl acetate; toluene; 1: Wittig olefination / 4: Swern oxidation / 5: Baeyer-Villiger oxidation;
DOI:10.1016/j.bmcl.2004.07.055