3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

Base Information

Chemical Name:3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one
CAS No.:182193-48-2
Molecular Formula:C₂₅H₃₆NO₃P
Molecular Weight:429.539
Hs Code.:

3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ<sup>5</sup>-[1,3]azaphosphinan-6-one

Synonyms:3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

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Chemical Property of 3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

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Technology Process of 3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

There total 6 articles about 3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-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:

: 768-90-1
1-Adamantyl bromide

: 182193-48-2
3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

Guidance literature:: Multi-step reaction with 3 steps

1: Ag₂O / CHCl₃ / 1.33 h / Heating

2: 96 percent / H₂ / Pd/C / aq. ethanol / 5 h

3: 4 N NaOH / aq. ethanol / 5 h

With sodium hydroxide; hydrogen; silver(l) oxide; palladium on activated charcoal; In ethanol; chloroform;
DOI:10.1021/jo9603439

Reference yield:

: 87438-94-6
ethyl 2-isobutylacrylate

: 182193-48-2
3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

Guidance literature:: Multi-step reaction with 4 steps

1: 1) hexamethyldisilazane / 1) 110 deg C, 1 h, 2) 90 deg C, 4 h

2: Ag₂O / CHCl₃ / 1.33 h / Heating

3: 96 percent / H₂ / Pd/C / aq. ethanol / 5 h

4: 4 N NaOH / aq. ethanol / 5 h

With sodium hydroxide; hydrogen; 1,1,1,3,3,3-hexamethyl-disilazane; silver(l) oxide; palladium on activated charcoal; In ethanol; chloroform;
DOI:10.1021/jo9603439

Reference yield:

: 115961-49-4
[2-phenyl-1-[[(phenylmethoxy)carbonyl]amino]ethyl]phosphinic acid

: 182193-48-2
3-(Adamantan-1-yloxy)-2-benzyl-5-isobutyl-3-oxo-3λ⁵-[1,3]azaphosphinan-6-one

Guidance literature:: Multi-step reaction with 4 steps

1: 1) hexamethyldisilazane / 1) 110 deg C, 1 h, 2) 90 deg C, 4 h

2: Ag₂O / CHCl₃ / 1.33 h / Heating

3: 96 percent / H₂ / Pd/C / aq. ethanol / 5 h

4: 4 N NaOH / aq. ethanol / 5 h

With sodium hydroxide; hydrogen; 1,1,1,3,3,3-hexamethyl-disilazane; silver(l) oxide; palladium on activated charcoal; In ethanol; chloroform;
DOI:10.1021/jo9603439