(5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol

Base Information

• Chemical Name: (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol
• CAS No.: 1435268-22-6
• Molecular Formula: C₂₂H₂₅ClO₆
• Molecular Weight: 420.89
• Mol file: 1435268-22-6.mol

Synonyms:(5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol

Chemical Property of (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol

There total 6 articles about (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol 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:

5,6-dimethoxy-2,2-dimethyl-2H-benzopyran (67015-34-3) + 2-(methoxymethoxy)-5-chlorobenzaldehyde (115560-38-8) → (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-7-yl)methanol (1435268-01-1) + (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol (1435268-22-6)

Guidance literature:

5,6-dimethoxy-2,2-dimethyl-2H-benzopyran; With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; In tetrahydrofuran; at 0 ℃; for 0.5h; Inert atmosphere;

2-(methoxymethoxy)-5-chlorobenzaldehyde; In tetrahydrofuran; at 0 - 20 ℃; for 7.5h; Overall yield = 38 %; Overall yield = 137 mg;

DOI:10.1016/j.bmc.2013.03.079

Reference yield:

2,4-Dihydroxybenzaldehyde (95-01-2) → (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-7-yl)methanol (1435268-01-1) + (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol (1435268-22-6)

Guidance literature:

Multi-step reaction with 5 steps

1.1: calcium hydroxide / methanol / 48 h / 20 °C

2.1: potassium carbonate / acetone / 20 h / 20 °C / Inert atmosphere

3.1: dihydrogen peroxide; potassium hydrogensulfate / methanol; water / 8 h / 20 °C

4.1: potassium carbonate / acetone / 20 h / Inert atmosphere; Reflux

5.1: N,N,N,N,-tetramethylethylenediamine; n-butyllithium / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

5.2: 7.5 h / 0 - 20 °C

With potassium hydrogensulfate; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; dihydrogen peroxide; potassium carbonate; calcium hydroxide; In tetrahydrofuran; methanol; water; acetone;

DOI:10.1016/j.bmc.2013.03.079

Reference yield:

5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde (54287-99-9) → (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-7-yl)methanol (1435268-01-1) + (5-chloro-2-(methoxymethoxy)phenyl)(5,6-dimethoxy-2,2-dimethyl-2H-benzopyran-8-yl)methanol (1435268-22-6)

Guidance literature:

Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 20 h / 20 °C / Inert atmosphere

2.1: dihydrogen peroxide; potassium hydrogensulfate / methanol; water / 8 h / 20 °C

3.1: potassium carbonate / acetone / 20 h / Inert atmosphere; Reflux

4.1: N,N,N,N,-tetramethylethylenediamine; n-butyllithium / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

4.2: 7.5 h / 0 - 20 °C

With potassium hydrogensulfate; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; dihydrogen peroxide; potassium carbonate; In tetrahydrofuran; methanol; water; acetone;

DOI:10.1016/j.bmc.2013.03.079

upstream raw materials:

2,4-Dihydroxybenzaldehyde

5-hydroxy-2,2-dimethyl-2H-chromene-6-carbaldehyde

3,3-dimethyl acrylaldehyde

5-(methoxy)-2,2-dimethyl-2H-chromene-6-carbaldehyde