Basic information Safety Supplier Related

1-(4-hydroxyphenyl)-2-methoxyethan-1-one

Basic information Safety Supplier Related

1-(4-hydroxyphenyl)-2-methoxyethan-1-one Basic information

Product Name:
1-(4-hydroxyphenyl)-2-methoxyethan-1-one
Synonyms:
  • 1-(4-hydroxyphenyl)-2-methoxyethan-1-one
  • 1-(4-Hydroxyphenyl)-2-methoxyethanone
  • 2-Methoxy-1-(4-hydroxyphenyl)ethanone
  • 2-Methoxy-4'-hydroxyacetophenone
  • Ethanone, 1-(4-hydroxyphenyl)-2-methoxy-
  • 2-Butenoicacid,2-hydroxy-4-[3-methyl-4-(phenylmethoxy)phenyl]-4-oxo-,methylester,(4Z)-
  • Alpha Methoxy -4-Hydroxy acetophenone
CAS:
32136-81-5
MF:
C9H10O3
MW:
166.17
EINECS:
250-929-2
Product Categories:
  • Aromatics
Mol File:
32136-81-5.mol
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1-(4-hydroxyphenyl)-2-methoxyethan-1-one Chemical Properties

Melting point:
128-130°C
Boiling point:
315.6±22.0 °C(Predicted)
Density 
1.168±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Acetone (Slightly), Methanol (Slightly)
form 
Solid
pka
7.84±0.15(Predicted)
color 
Light Orange to Light Brown
InChI
InChI=1S/C9H10O3/c1-12-6-9(11)7-2-4-8(10)5-3-7/h2-5,10H,6H2,1H3
InChIKey
HUXGFSJRCMJOAK-UHFFFAOYSA-N
SMILES
C(=O)(C1=CC=C(O)C=C1)COC
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Safety Information

HS Code 
2914500090
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1-(4-hydroxyphenyl)-2-methoxyethan-1-one Usage And Synthesis

Chemical Properties

Tan Solid

Uses

2-Methoxy-4''-hydroxyacetophenone (cas# 32136-81-5) is a compound useful in organic synthesis.

Preparation

Obtained by scission of 5-hydroxy-4-(4-hydroxyphenyl) 5H-furan-2-one with potassium hydroxide in methanol at 20° for 24 h (85%). – Also obtained by catalytic debenzylation of 1-(4-benzyloxyphenyl)-2-methoxyethanone in methanol under hydrogen (five bars) in the presence of 5% Pd/C for 24 h (81%).

Synthesis

2491-38-5

32136-81-5

General procedure for the synthesis of 1-(4-hydroxyphenyl)-2-methoxyacetophenone from 2-bromo-1-(4-hydroxyphenyl)acetophenone: Example 3 Preparation of α-methoxy-4-hydroxyacetophenone. Dissolve 2 g of α-bromo-4-hydroxyacetophenone in 11 g of methanol. 30g of methanol solution of saturated sodium hydroxide (1g NaOH dissolved in 4.2ml methanol) was slowly added dropwise to the above solution. Upon completion of the dropwise addition, the reaction mixture was poured into 30 g of ice water and the pH was adjusted with acid to 6. Subsequently, α-methoxy-4-hydroxyacetophenone precipitated as a precipitate, and after filtration and drying, a yellowish-green product was obtained in about 85% yield. The purity of the product was confirmed by 1H-NMR analysis.

References

[1] Patent: US5107034, 1992, A

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