1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

Base Information

Chemical Name:1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one
CAS No.:865084-86-2
Molecular Formula:C₆₀H₅₃NO₈
Molecular Weight:916.083
Hs Code.:

1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-<i>c</i>]oxazol-3-one

Synonyms:1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

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Chemical Property of 1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

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Technology Process of 1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

There total 4 articles about 1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one 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: 89.0%

: 865084-84-0
1,1-bis-(4-hydroxy-phenyl)-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

: 24131-32-6
3,5-bis(benzyloxy)benzyl bromide

: 865084-86-2
1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

Guidance literature:: With 18-crown-6 ether; potassium carbonate; In acetone; at 20 ℃; for 18h;
DOI:10.1021/jo050994h

Reference yield:

: 865084-83-9
1,1-bis-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

: 865084-86-2
1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / TBAF / tetrahydrofuran / 5 h / cooling

2: 89 percent / K₂CO₃; 18-crown-6 / acetone / 18 h / 20 °C

With 18-crown-6 ether; tetrabutyl ammonium fluoride; potassium carbonate; In tetrahydrofuran; acetone;
DOI:10.1021/jo050994h

Reference yield:

: 67963-68-2
t-butyldimethylsilyl-4-bromophenol

: 865084-86-2
1,1-bis-[4-(3,5-bis-benzyloxy-benzyloxy)-phenyl]-tetrahydro-pyrrolo[1,2-c]oxazol-3-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: Mg; I₂ / tetrahydrofuran / 1 h / Heating

1.2: 44 percent / tetrahydrofuran / 2 h / Heating

2.1: 90 percent / TBAF / tetrahydrofuran / 5 h / cooling

3.1: 89 percent / K₂CO₃; 18-crown-6 / acetone / 18 h / 20 °C

With 18-crown-6 ether; tetrabutyl ammonium fluoride; iodine; potassium carbonate; magnesium; In tetrahydrofuran; acetone;
DOI:10.1021/jo050994h