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Potassium Carbonate → N'-(5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)hydrazinecarboxylic acid 4-methoxy-benzyl ester

HRID 229972
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 229972
[C:1]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[CH:9][CH:8]=1)(=[O:4])[NH:2][NH2:3].C(=O)([O-])[O-].[K+].[K+].[CH3:21][C:22]1[C:31]2[O:30][CH2:29][CH2:28][O:27][C:26]=2[CH:25]=[CH:24][C:23]=1[C:32](Cl)=[O:33]>C(Cl)Cl.O>[CH3:14][O:13][C:10]1[CH:11]=[CH:12][C:7]([CH2:6][O:5][C:1]([NH:2][NH:3][C:32]([C:23]2[CH:24]=[CH:25][C:26]3[O:27][CH2:28][CH2:29][O:30][C:31]=3[C:22]=2[CH3:21])=[O:33])=[O:4])=[CH:8][CH:9]=1
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Komponenten

6

Edukt 3

HCID 11430Potassium CarbonateHCID 87847p-Methoxybenzyl carbazateHCID 107749295-Methyl-2,3-dihydro-1,4-benzodioxine-6-carbonyl chloride

Produkt 1

HCID 59838614N'-(5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)hydrazinecarboxylic acid 4-methoxy-benzyl ester

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittel
2×
HCID 6344DichloromethaneLösungsmittel3×

Versuchsvorschrift

17.8 5 g (90.98 mmol) of 4-methoxybenzyl carbazate was dissolved in 50 mL of CH2Cl2 in a 250 mL flask and then cooled in ice water. 21.42 g (155 mmol) of potassium carbonate dissolved in 80 mL of water was added. While the reaction mixture was being stirred in the ice bath, 17.0 g (79.95 mmol) of 5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl chloride in 60 mL of CH2Cl2 were slowly added. The reaction mixture was stirred at room temperature overnight and then transferred to a separatory funnel with 200 mL of CH2Cl2 and 200 mL of H2O. After shaking, a floating white precipitate was filtered off, washed with water, dried in a vacuum oven to give 29.1 g of N′-(5-methyl-2,3-dihydro-benzo[1,4]dioxine-6-carbonyl)hydrazinecarboxylic acid 4-methoxy-benzyl ester. The CH2Cl2 solution was dried and concentrated to give 5.19 g of a residue consisting of the original acid chloride, 4-methoxybenzyl carbazate, and some product. TLC Rf=0.38 (streak 1:1 ethyl acetate:hexane). 1H NMR (CDCl3, 300 MHz) δ (ppm): 7.4-6.7 (m, 6H), 5.139 (s 2H), 4.279 (s 4H), 3.81 (s, 3H), 2.303 (s, 3H).

Aufarbeitung

  1. additionwas added
  2. additionwere slowly added
  3. stirringAfter shaking
  4. filtrationa floating white precipitate was filtered off
  5. washwashed with water
  6. customdried in a vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-2ed72f2bfd2d4a51b5407ebc803087a3
Quelldatensatz
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07563928B2

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