2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

Base Information

Chemical Name:2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene
CAS No.:910106-22-8
Molecular Formula:C₃₁H₃₅NO₂
Molecular Weight:453.624
Hs Code.:

2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2<i>H</i>,4b<i>H</i>-10-oxa-4a-aza-indeno[1,2-<i>a</i>]indene

Synonyms:2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

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Chemical Property of 2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

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Technology Process of 2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

There total 6 articles about 2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene 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: 97.0%

: 910106-21-7
(5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]inden-2-yl)-methanol

: 100-39-0
benzyl bromide

: 910106-22-8
2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1021/ol0614065

Reference yield:

: 461640-97-1
(1S,2R)-(-)-cis-1-amino-7-isopropylindan-2-ol

: 910106-22-8
2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / 4 Angstroem molecular sieves; LiCl; P(2-furyl)3 / tris(dibenzylideneacetone)dipalladium⁽⁰⁾ / dimethylformamide / 1 h / 80 °C

2: 52 percent / Mg / 3 h / 20 °C

3: 99 percent / Red-Al(R) / toluene / 2 h / 0 °C

4: 97 percent / NaH / dimethylformamide / 4 h / 20 °C

With trifuran-2-yl-phosphane; 4 A molecular sieve; sodium hydride; magnesium; sodium bis(2-methoxyethoxy)aluminium dihydride; lithium chloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In N,N-dimethyl-formamide; toluene;
DOI:10.1021/ol0614065

Reference yield:

: 66680-87-3,66680-88-4,79159-76-5
(E)-1-phenyl-(2-tributylstannyl)ethene

: 910106-22-8
2-benzyloxymethyl-5-isopropyl-4-phenyl-1,3,4,9,9a,10a-hexahydro-2H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene

Guidance literature:: Multi-step reaction with 4 steps

1: 84 percent / 4 Angstroem molecular sieves; LiCl; P(2-furyl)3 / tris(dibenzylideneacetone)dipalladium⁽⁰⁾ / dimethylformamide / 1 h / 80 °C

2: 52 percent / Mg / 3 h / 20 °C

3: 99 percent / Red-Al(R) / toluene / 2 h / 0 °C

4: 97 percent / NaH / dimethylformamide / 4 h / 20 °C

With trifuran-2-yl-phosphane; 4 A molecular sieve; sodium hydride; magnesium; sodium bis(2-methoxyethoxy)aluminium dihydride; lithium chloride; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In N,N-dimethyl-formamide; toluene;
DOI:10.1021/ol0614065