2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

Base Information

Chemical Name:2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol
CAS No.:1431533-72-0
Molecular Formula:C₁₇H₁₈ClNO₃
Molecular Weight:319.788
Hs Code.:

Synonyms:2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

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Chemical Property of 2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

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Technology Process of 2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

There total 7 articles about 2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol 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:

: 1431533-71-9
2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-6,7-dihydro-4H-spiro[1,3-benzoxazole-5,2'-[1,3]dioxolane]

: 1431533-72-0
2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

Guidance literature:: 2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-6,7-dihydro-4H-spiro[1,3-benzoxazole-5,2'-[1,3]dioxolane]; With hydrogenchloride; In tetrahydrofuran; methanol; water; at 70 ℃; for 1h;

With methanol; sodium tetrahydroborate; In tetrahydrofuran; ethyl acetate; at 20 ℃; for 0.333333h;

Reference yield:

: 34989-52-1
(+/-)-spiro[1,3-dioxolane-2,3'-[7]oxabicyclo[4.1.0]heptane]

: 1431533-72-0
2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

Guidance literature:: Multi-step reaction with 5 steps

1.1: isopropyl alcohol / 90 °C

2.1: hydrogen; palladium 10% on activated carbon / water; ethanol / 2 h / 20 °C / 3800.26 Torr

3.1: oxalyl dichloride; N,N-dimethyl-formamide / water; ethanol / 0.5 h / 20 °C

3.2: 0.5 h / 20 °C

4.1: sulfur trioxide pyridine complex; triethylamine / dimethyl sulfoxide / 1 h / Inert atmosphere

4.2: 1 h / 60 °C

5.1: hydrogenchloride / methanol; tetrahydrofuran; water / 1 h / 70 °C

5.2: 0.33 h / 20 °C

With hydrogenchloride; oxalyl dichloride; palladium 10% on activated carbon; hydrogen; sulfur trioxide pyridine complex; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; ethanol; water; dimethyl sulfoxide; isopropyl alcohol;

Reference yield:

: 1431533-70-8
3-chloro-4-(cyclopropylmethoxy)-N-(8-hydroxy-1,4-dioxaspiro[4.5]dec-7-yl)benzamide

: 1431533-72-0
2-(3-chloro-4-(cyclopropylmethoxy)phenyl)-4,5,6,7-tetrahydro-1,3-benzoxazol-5-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: sulfur trioxide pyridine complex; triethylamine / dimethyl sulfoxide / 1 h / Inert atmosphere

1.2: 1 h / 60 °C

2.1: hydrogenchloride / methanol; tetrahydrofuran; water / 1 h / 70 °C

2.2: 0.33 h / 20 °C

With hydrogenchloride; sulfur trioxide pyridine complex; triethylamine; In tetrahydrofuran; methanol; water; dimethyl sulfoxide;