(4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

Base Information

Chemical Name:(4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone
CAS No.:1394030-05-7
Molecular Formula:C₂₈H₃₇NO₅
Molecular Weight:467.605
Hs Code.:

Synonyms:(4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

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Chemical Property of (4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

Chemical Property:

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Technology Process of (4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

There total 7 articles about (4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone 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:

: 19099-93-5
benzyl 4-oxo-1-piperidinecarboxylate

: 1394030-05-7
(4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyrrolidine / methanol / 20 h / 80 °C

2.1: hydrogen / palladium 10% on activated carbon / isopropyl alcohol / 25 °C

3.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 16 h / 20 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.67 h / -78 °C

4.2: -78 - 20 °C

5.1: sodium tetrahydroborate; methanol / 0.5 h / 0 - 20 °C

6.1: potassium tetrachloroaurate(III) / 48 h / 70 °C

With pyrrolidine; methanol; sodium tetrahydroborate; potassium tetrachloroaurate(III); hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; isopropyl alcohol;

Reference yield:

: 1394030-83-1
(4-hydroxy-3-methylspiro[chroman-2,4'-piperidine]-1'-yl)(4-isopropoxy-3-methoxyphenyl)methanone

: 75-65-0
tert-butyl alcohol

: 1394030-05-7
(4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

Guidance literature:: With potassium tetrachloroaurate(III); at 70 ℃; for 48h;

Reference yield:

: 118-93-4,104809-67-8
o-hydroxyacetophenone

: 1394030-05-7
(4-tert-butoxyspiro[chromane-2,4'-piperidine]-1'-yl)-(4-isopropoxy-3-methoxyphenyl)-methanone

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyrrolidine / methanol / 20 h / 80 °C

2.1: hydrogen / palladium 10% on activated carbon / isopropyl alcohol / 25 °C

3.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 16 h / 20 °C

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.67 h / -78 °C

4.2: -78 - 20 °C

5.1: sodium tetrahydroborate; methanol / 0.5 h / 0 - 20 °C

6.1: potassium tetrachloroaurate(III) / 48 h / 70 °C

With pyrrolidine; methanol; sodium tetrahydroborate; potassium tetrachloroaurate(III); hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; isopropyl alcohol;