Sodium Iodide → 3-Iodo-2-propynyl butylcarbamate

HRID 404987

Reaktionsgleichung

Reaktionsgleichung von HRID 404987
[CH2:1]([NH:5][C:6](=[O:11])[O:7][CH2:8][C:9]#[CH:10])[CH2:2][CH2:3][CH3:4].[OH-].[Na+].[I-:14].[Na+].ClCl>O.CO>[CH2:1]([NH:5][C:6](=[O:11])[O:7][CH2:8][C:9]#[C:10][I:14])[CH2:2][CH2:3][CH3:4]

Komponenten

7

Edukt 4

HCID 5238Sodium IodideHCID 14798Sodium HydroxideHCID 24526ChlorineHCID 108773542-Propynyl butylcarbamate

Produkt 1

HCID 620973-Iodo-2-propynyl butylcarbamateAusbeute 84,9 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel2×

Versuchsvorschrift

At 5° C., 19.0 g of propargyl butylcarbamate (0.122 mol), 12.2 g of sodium hydroxide (0.305 mol) and 18.5 g of sodium iodide (0.123 mol) are introduced as initial charge in 50 g of water and 48 g of methanol. Chlorine (11.7 g, 0.165 mmol) is then slowly introduced so that the temperature remains below 5° C. When the metered addition is complete, the mixture is stirred at this temperature for 1 h, then slowly heated to room temperature and stirred for 1 hour. After adding 100 g of water, the precipitated solid is isolated by filtration, washed with water and dried in vacuo. This gives 29.1 g of 3-iodo-2-propynyl N-butylcarbamate (purity: 94.7% (HPLC), polyiodized compounds: <0.1% (HPLC), yield: 80%).

Aufarbeitung

  1. customremains below 5° C
  2. additionWhen the metered addition
  3. stirringstirred for 1 hour
  4. customthe precipitated solid is isolated by filtration
  5. washwashed with water
  6. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-a1583321215b4e15adbd70039e6dd200
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08748652B2

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