2-Bromo-6-(prop-2-en-1-yl)phenol

Base Information

• Chemical Name: 2-Bromo-6-(prop-2-en-1-yl)phenol
• CAS No.: 17269-81-7
• Molecular Formula: C9H9BrO
• Molecular Weight: 213.074
• DSSTox Substance ID: DTXSID00529180
• Nikkaji Number: J3.425.552K
• Wikidata: Q82399402
• Mol file: 17269-81-7.mol

Synonyms:17269-81-7;Phenol, 2-bromo-6-(2-propenyl)-;2-Bromo-6-(prop-2-en-1-yl)phenol;2-allyl-6-bromophenol;2-bromo-6-prop-2-enylphenol;2-allyl-6-bromo-phenol;SCHEMBL430415;DTXSID00529180;PTJOFMJOMTXHGU-UHFFFAOYSA-N;AKOS011655080;EN300-76268;G28766

Chemical Property of 2-Bromo-6-(prop-2-en-1-yl)phenol

Chemical Property:

• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 211.98368
• Heavy Atom Count: 11
• Complexity: 136

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CCC1=C(C(=CC=C1)Br)O

Technology Process of 2-Bromo-6-(prop-2-en-1-yl)phenol

There total 5 articles about 2-Bromo-6-(prop-2-en-1-yl)phenol 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%

O-allyl-2-bromophenol (60333-75-7) → 2-bromo-6-(2-propenyl)phenol (17269-81-7)

Guidance literature:

With diethylaluminium chloride; In hexane;

DOI:10.1016/S0040-4039(00)01121-7

Reference yield: 100.0%

2-hydroxybromobenzene (95-56-7) + allyl bromide (106-95-6) → 2-bromo-6-(2-propenyl)phenol (17269-81-7)

Guidance literature:

2-hydroxybromobenzene; allyl bromide; With potassium carbonate; In acetone; for 4h; Heating;

at 200 ℃; for 1.1h; Further stages.; microwave irradiation;

DOI:10.1016/j.bmc.2007.07.010

Reference yield:

2-hydroxybromobenzene (95-56-7) → 2-bromo-6-(2-propenyl)phenol (17269-81-7)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 2.5 h / Heating

2: 7.6 g / 200 - 220 °C

With potassium carbonate; In acetone;

DOI:10.1016/j.tet.2005.12.026

upstream raw materials:

O-allyl-2-bromophenol

2-hydroxybromobenzene

allyl bromide

o-Allylphenol

Downstream raw materials:

3-Brom-2-methoxy-1-(2-propenyl)benzol

7-bromo-2-hydroxymethyl-2,3-dihydrobenzo[b]furan

(3-bromo-2-hydroxyphenyl)acetaldehyde

3-bromo-2-methyloxybenzaldehyde