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ChemicalBook CAS DataBase List 2-Pyridylamid oxime
1772-01-6

2-Pyridylamid oxime synthesis

4synthesis methods
-

Yield:1772-01-6 100%

Reaction Conditions:

with hydroxyamino hydrochloride;triethylamine in ethanol; for 3 h;Reflux;

Steps:

Amidoxime Intermediate

2-Pyridinecarboximidamide, N-Hydroxy-
Amidoxime Intermediate
To a 1 L single neck round-bottomed flask equipped with a stir bar were charged 40 g (384 mmol) of 2-pyridinecarbonitrile, 26.7 g (384 mmol) of hydroxylamine hydrochloride, 107 mL (768 mmol) of triethylamine and 300 mL of ethanol.
The flask was fitted with a reflux condenser and the mixture heated under reflux for three hours (TLC showed no remaining starting material).
After concentration on a rotary evaporator, the residue was slurried in a mixture of 300 mL of dichloromethane and 300 mL of water.
The slurry was filtered and the product cake washed several times with water.
The organic layer washed with 2*300 mL of water.
The aqueous layers were backwashed with 50 mL of dichloromethane and the combined organic layers dried over magnesium sulfate, filtered and rotary evaporated, giving a white solid.
The solids were combined and dried in a reduced pressure oven, giving 52.5 g (100%) of product, m.p. 116° C. 1H NMR (400 MHz, DMSO-d6) 9.9 (s, 1H, -OH), 8.53 (m, 1H, Ar-H), 7.85 (d, 1H, Ar-H), 7.78 (t, 1H, Ar-H), 7.38 (m, 1H, Ar-H), 5.82 (br s, 2H, -NH2), 1.90-0.85 (m, 19H, aliphatics).

References:

US2016/244860,2016,A1 Location in patent:Paragraph 0144-0145

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