1-Benzyloxy-4-bromomethyl-2-chloro-benzene

Base Information

Chemical Name:1-Benzyloxy-4-bromomethyl-2-chloro-benzene
CAS No.:536974-88-6
Molecular Formula:C14H12BrClO
Molecular Weight:311.606
Hs Code.:
DSSTox Substance ID:DTXSID301232053
Mol file:536974-88-6.mol

Synonyms:536974-88-6;SCHEMBL3240051;VPPPBXQHZBIXGC-UHFFFAOYSA-N;DTXSID301232053;AKOS012844209;1-Benzyloxy-4-bromomethyl-2-chloro-benzene;4-(Bromomethyl)-2-chloro-1-(phenylmethoxy)benzene

Suppliers and Price of 1-Benzyloxy-4-bromomethyl-2-chloro-benzene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-Benzyloxy-4-bromomethyl-2-chloro-benzene

Chemical Property:

XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:309.97601
Heavy Atom Count:17
Complexity:218

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=C(C=C(C=C2)CBr)Cl

Technology Process of 1-Benzyloxy-4-bromomethyl-2-chloro-benzene

There total 4 articles about 1-Benzyloxy-4-bromomethyl-2-chloro-benzene 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%

: 536974-87-5
(4-benzyloxy-3-chlorophenyl)methanol

: 536974-88-6
1-benzyloxy-4-bromomethyl-2-chlorobenzene

Guidance literature:: With phosphorus tribromide; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1021/jm061462b

Reference yield:

: 2420-16-8
4-hydroxy-3-chlorobenzaldehyde

: 536974-88-6
1-benzyloxy-4-bromomethyl-2-chlorobenzene

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / K₂CO₃ / dimethylformamide

2: 89 percent / NaBH₄ / ethanol; tetrahydrofuran / 0 - 20 °C

3: 100 percent / PBr₃ / CH₂Cl₂ / 1 h / 0 °C

With sodium tetrahydroborate; phosphorus tribromide; potassium carbonate; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm061462b

Reference yield:

: 66422-84-2
4-benzyloxy-3-chlorobenzaldehyde

: 536974-88-6
1-benzyloxy-4-bromomethyl-2-chlorobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / NaBH₄ / ethanol; tetrahydrofuran / 0 - 20 °C

2: 100 percent / PBr₃ / CH₂Cl₂ / 1 h / 0 °C

With sodium tetrahydroborate; phosphorus tribromide; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/jm061462b