2-(Benzyloxy)-4-methoxy-6-methylbenzoyl chloride

Base Information

• Chemical Name: 2-(Benzyloxy)-4-methoxy-6-methylbenzoyl chloride
• CAS No.: 65857-79-6
• Molecular Formula: C₁₆H₁₅ClO₃
• Molecular Weight: 290.746
• DSSTox Substance ID: DTXSID40501081
• Wikidata: Q82353201

Synonyms:65857-79-6;2-(Benzyloxy)-4-methoxy-6-methylbenzoyl chloride;DTXSID40501081

Chemical Property of 2-(Benzyloxy)-4-methoxy-6-methylbenzoyl chloride

Chemical Property:

• XLogP3: 4.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 290.0709720
• Heavy Atom Count: 20
• Complexity: 315

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC(=CC(=C1C(=O)Cl)OCC2=CC=CC=C2)OC

Technology Process of 2-(Benzyloxy)-4-methoxy-6-methylbenzoyl chloride

There total 3 articles about 2-(Benzyloxy)-4-methoxy-6-methylbenzoyl chloride 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:

2-hydroxy-4-methoxy-6-methylbenzoic acid (570-10-5) → 2-benzyloxy-4-methoxy-6-methylbenzyl chloride (65857-79-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 95 percent / K₂CO₃ / acetone / 48 h / Heating

2: 90 percent / KOH / ethanol / 2 h / Heating

3: thionyl chloride / 2 h / Heating

With potassium hydroxide; thionyl chloride; potassium carbonate; In ethanol; acetone;

DOI:10.1039/P19810002710

Reference yield:

benzyl 2-benzyloxy-4-methoxy-6-methylbenzoate (68048-10-2) → 2-benzyloxy-4-methoxy-6-methylbenzyl chloride (65857-79-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent / KOH / ethanol / 2 h / Heating

2: thionyl chloride / 2 h / Heating

With potassium hydroxide; thionyl chloride; In ethanol;

DOI:10.1039/P19810002710

Reference yield:

2-benzyloxy-4-methoxy-6-methylbenzoic acid (68048-09-9) → 2-benzyloxy-4-methoxy-6-methylbenzyl chloride (65857-79-6)

Guidance literature:

With thionyl chloride; for 2h; Heating;

DOI:10.1039/P19810002710

upstream raw materials:

2-benzyloxy-4-methoxy-6-methylbenzoic acid

2-hydroxy-4-methoxy-6-methylbenzoic acid

benzyl 2-benzyloxy-4-methoxy-6-methylbenzoate

Downstream raw materials:

1,3-bis(benzyloxy)-6,8-bis-(2-benzyloxy-4-methoxy-6-methylbenzoyloxy)naphthalene

1,3-bis(benzyloxy)-6-(2-benzyloxy-4-methoxy-6-methylbenzoyloxy)-8-hydroxynaphthalene

8,10-bis(benzyloxy)-11-hydroxy-3-methoxy-1-methylbenzoxanthen-12-one

1,3-bis(benzyloxy)-6-hydroxy-10-methoxy-8-methylbenzoxanthen-7-one

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