2-(Benzyloxy)-4-(bromomethyl)-1-methoxybenzene

Base Information

• Chemical Name: 2-(Benzyloxy)-4-(bromomethyl)-1-methoxybenzene
• CAS No.: 55667-12-4
• Molecular Formula: C15H15BrO2
• Molecular Weight: 307.187
• European Community (EC) Number: 676-364-5
• DSSTox Substance ID: DTXSID30471502
• Wikidata: Q82300021
• Mol file: 55667-12-4.mol

Synonyms:2-(Benzyloxy)-4-(bromomethyl)-1-methoxybenzene;55667-12-4;4-(bromomethyl)-1-methoxy-2-phenylmethoxybenzene;SCHEMBL2060386;DTXSID30471502;JLKLAWVKJNTSAB-UHFFFAOYSA-N;MFCD10687131;BS-28533;2-benzyloxy-4-bromomethyl-1-methoxybenzene;FT-0736402;A913322;A1-01223

Chemical Property of 2-(Benzyloxy)-4-(bromomethyl)-1-methoxybenzene

Chemical Property:

• Vapor Pressure: 0mmHg at 25°C
• Melting Point: 94.5 °C
• Refractive Index: 1.589
• Boiling Point: 390.68°C at 760 mmHg
• Flash Point: 167.644°C
• PSA: 18.46000
• Density: 1.349g/cm³
• LogP: 4.16910
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 306.02554
• Heavy Atom Count: 18
• Complexity: 229

Purity/Quality:

99%, ^*data from raw suppliers

2-Benzyloxy-4-bromomethyl-1-methoxybenzene 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC1=C(C=C(C=C1)CBr)OCC2=CC=CC=C2

Technology Process of 2-(Benzyloxy)-4-(bromomethyl)-1-methoxybenzene

There total 9 articles about 2-(Benzyloxy)-4-(bromomethyl)-1-methoxybenzene 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: 100.0%

→ 4-methoxy-3-(benzyloxy)benzyl bromide (55667-12-4)

Guidance literature:

Reference yield: 96.0%

3-benzyloxy-4-methoxy-benzyl alcohol (1860-60-2) → 4-methoxy-3-(benzyloxy)benzyl bromide (55667-12-4)

Guidance literature:

With phosphorus tribromide; In tetrahydrofuran; at 0 ℃; for 1.5h;

Reference yield:

3-benzyloxy-4-methoxybenzaldehyde (6346-05-0) → 4-methoxy-3-(benzyloxy)benzyl bromide (55667-12-4)

Guidance literature:

Multi-step reaction with 2 steps

1: NaBH₄ / tetrahydrofuran; ethanol / 0 - 20 °C

2: PBr₃ / CH₂Cl₂ / 0 °C

With sodium tetrahydroborate; phosphorus tribromide; In tetrahydrofuran; ethanol; dichloromethane;

DOI:10.1021/jm061462b

upstream raw materials:

3-benzyloxy-4-methoxy-benzyl alcohol

3-benzyloxy-4-methoxybenzaldehyde

isovanillin

benzyl bromide

Downstream raw materials:

arctigenin

2-(3-Benzyloxy-4-methoxy-benzyl)-2-(3,4,5-trimethoxy-phenyl)-[1,3]dithiane

(+/-)-Prestegane B

(3R^*,4R^*)-3-(3-benzoxy-4-methoxybenzyl)-4-(3-benzoxy-4-methoxybenzyl)-4,5-dihydro-2(3H)-furanone

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