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ChemicalBook CAS DataBase List 3,5-Dihydroxyacetophenone
51863-60-6

3,5-Dihydroxyacetophenone synthesis

5synthesis methods
Preparation from 3,5-dimethoxyacetophenone (SM) by demethylation with aluminium chloride in refluxing chlorobenzene (71%) The starting material (SM) was prepared by a three-step procedure from 3,5-dimethoxy-benzoic acid.
35086-59-0 Synthesis
3,5-Diacetoxyacetophenone

35086-59-0
200 suppliers
$5.00/1g

-

Yield:-

Reaction Conditions:

with immobilized Burkholderia cepacia lipase (Amano PS-IM) in tetrahydrofuran;isopropyl alcohol at 20; for 60 h;Inert atmosphere;Enzymatic reaction;

Steps:

1 2.1 1-(3,5-Dihydroxyphenyl)ethanone (3a)
For a preparative scale-reaction, the commercially available 3b (5.32 g, 22.5 mmol) showed smell of acetic acid, and prior to use, it was evacuated in a 200-mL brown-colored recovery flask with for 30 min at 20 mmHg. Then it was diluted with a mixture of 2-propanol (25 mL) and tetrahydrofuran (THF, 50 mL) and lipase PS-IM (2.5 g) was added. The mixture was stirred for 60 h at room temperature under argon atmosphere. After recovery of lipase by suction filtration, the filtrate was concentrated in vacuo to give 3a (3.52 g, quant) as solid. 1H NMR (500 MHz, CDCl3): δ 2.55 (s, 3H), 6.56 (t, J = 2.5 Hz, 1H), 6.99 (d, J = 2.5 Hz, 2H). Its NMR spectrum was identical with that of an authentic sample. This was employed for the next step without further purification. The recovered lipase was effectively active, after storage in a refrigerator for 2 months.

References:

Asami, Kento;Machida, Takuya;Jung, Sonna;Hanaya, Kengo;Shoji, Mitsuru;Sugai, Takeshi [Journal of Molecular Catalysis B: Enzymatic,2013,vol. 97,p. 106 - 109]

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