4-BENZYLOXY-2-METHOXYBENZALDEHYDE

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Products Intro: Product Name:4-Benzyloxy-2-methoxybenzaldehyde
CAS:58026-14-5
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Products Intro: Product Name:4-(Benzyloxy)-2-methoxybenzaldehyde
CAS:58026-14-5
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Products Intro: Product Name:4-(Benzyloxy)-2-methoxybenzaldehyde
CAS:58026-14-5
Purity:NLT 98% Remarks:MC561604
4-BENZYLOXY-2-METHOXYBENZALDEHYDE Basic information
Product Name:4-BENZYLOXY-2-METHOXYBENZALDEHYDE
Synonyms:2-methoxy-4-benzyloxybenzaldehyde;4-BENZYLOXY-2-METHOXYBENZALDEHYDE;4-Benzyloxy-o-anisaldehyde;4-BENZYLOXY-2-METHOXYBENZALDEHYDE, 98+%;2-Methoxy-4-(phenylMethoxy)benzaldehyde;5-(Benzyloxy)-2-formylanisole;Benzaldehyde, 2-methoxy-4-(phenylmethoxy)-
CAS:58026-14-5
MF:C15H14O3
MW:242.27
EINECS:
Product Categories:Phenyls & Phenyl-Het;Aromatics;Aldehydes;Phenyls & Phenyl-Het
Mol File:58026-14-5.mol
4-BENZYLOXY-2-METHOXYBENZALDEHYDE Structure
4-BENZYLOXY-2-METHOXYBENZALDEHYDE Chemical Properties
Melting point 98-100°C
Boiling point 180°C 2mm
density 1.154±0.06 g/cm3(Predicted)
Fp 180°C/2mm
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
AppearanceLight yellow to brown Solid
Sensitive Air Sensitive
BRN 1880700
CAS DataBase Reference58026-14-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Safety Statements 22-24/25
HS Code 2912490090
MSDS Information
ProviderLanguage
ALFA English
4-BENZYLOXY-2-METHOXYBENZALDEHYDE Usage And Synthesis
Synthesis
4-Hydroxy-2-methoxybenzaldehyde

18278-34-7

Benzyl bromide

100-39-0

4-BENZYLOXY-2-METHOXYBENZALDEHYDE

58026-14-5

4-Hydroxy-2-methoxybenzaldehyde (200 mg, 1.31 mmol) was dissolved in N,N-dimethylformamide (DMF) under the protection of nitrogen (N2), potassium carbonate (K2CO3, 543 mg, 3.93 mmol) was added, and stirred for 30 min at room temperature. Subsequently, benzyl bromide (BnBr, 0.312 mL, 2.62 mmol) was added dropwise to the reaction mixture and stirring was continued for 1.5 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate (EtOAc) and washed with deionized water (H2O). The organic phase was dried with anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. Purification by silica gel column chromatography with ethyl acetate/hexane (1:2, v/v) as eluent afforded the target product 4-benzyloxy-2-methoxybenzaldehyde (304 mg, 95.7% yield).1H-NMR (CDCl3, 400 MHz) δ: 7.81 (d, 1H, J = 8.6 Hz), 7.36 (m, 5H), 6.62 ( dd, 1H, J = 8.7, 2.2 Hz), 6.54 (d, 1H, J = 2.2 Hz), 5.14 (s, 2H), 3.89 (s, 3H).

References[1] Molecules, 2015, vol. 20, # 9, p. 15966 - 15975
[2] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 9, p. 1429 - 1437
[3] Journal of the American Chemical Society, 2006, vol. 128, # 33, p. 10640 - 10641
[4] Patent: WO2006/40520, 2006, A1. Location in patent: Page/Page column 103
[5] Patent: WO2007/99326, 2007, A1. Location in patent: Page/Page column 111
4-BENZYLOXY-2-METHOXYBENZALDEHYDE Preparation Products And Raw materials
Raw materialsIodomethane-->4-Hydroxy-2-methoxybenzaldehyde-->Benzyl bromide-->4-BENZYLOXY-2-HYDROXYBENZALDEHYDE-->Potassium carbonate-->N,N-Dimethylformamide
Tag:4-BENZYLOXY-2-METHOXYBENZALDEHYDE(58026-14-5) Related Product Information
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