tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

Base Information

Chemical Name:tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate
CAS No.:1355091-05-2
Molecular Formula:C₂₆H₃₂ClNO₄
Molecular Weight:457.997
Hs Code.:

Synonyms:tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

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Chemical Property of tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

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Technology Process of tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

There total 7 articles about tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate 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:

: 17849-38-6
2-Chlorobenzyl alcohol

: 1355088-07-1
tert-butyl 3-[6-hydroxy-2H-spiro(1-benzofuran-3,4'-piperidine)-1'-yl]propanoate

: 1355091-05-2
tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1016/j.bmcl.2017.12.018

Reference yield:

: 1355087-61-4
1'-benzyl-2H-spiro(1-benzofuran-3,4'-piperidin)-6-ol

: 1355091-05-2
tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen; palladium(II) hydroxide; hydrogenchloride / water; methanol / 48 h / 20 °C

2: diisopropylamine / methanol / Reflux

3: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 16 h / 20 °C

With hydrogenchloride; di-isopropyl azodicarboxylate; hydrogen; palladium(II) hydroxide; diisopropylamine; triphenylphosphine; In methanol; dichloromethane; water; 3: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2017.12.018

Reference yield:

: 1663-39-4,25232-27-3
tert-Butyl acrylate

: 1355091-05-2
tert-butyl 3-{6-[(2-chlorophenyl)methoxy]-2H-spiro[1-benzofuran-3,4'-piperidine]-1'-yl}propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: diisopropylamine / methanol / Reflux

2: triphenylphosphine; di-isopropyl azodicarboxylate / dichloromethane / 16 h / 20 °C

With di-isopropyl azodicarboxylate; diisopropylamine; triphenylphosphine; In methanol; dichloromethane; 2: |Mitsunobu Displacement;
DOI:10.1016/j.bmcl.2017.12.018