Hydrochloric Acid → HCID 13393461, Verbindung
Reaktionsgleichung
[OH:1][C:2]1[CH:10]=[CH:9][C:8]([C:11](=[O:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[BH4-].[Na+].Cl>C(O)C>[OH:1][C:2]1[CH:10]=[CH:9][C:8]([CH:11]([OH:29])[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-Hydroxy-5-(1-oxooctadecyl)benzoic acid (1.0 g) was added to 5 ml absolute ethanol, followed by 94 mg of NaBH4. The mixture was stirred at room temperature for 2 hours, then added to 10 ml of 0.1N HCl to give a solid. The solid was filtered, washed with 10 ml of water, dried in air and then at a pressure of 0.5 mm Hg at room temperature for about 65 hours to give the title compound, m.p. ca. 102° C. ##STR10##
Aufarbeitung
- customto give a solid
- filtrationThe solid was filtered
- washwashed with 10 ml of water
- customdried in air
Quellen und Nachweise
- ORD-Eintrag
- ord-91add2c63d6e4725af915ce3cb43599f
- Quelldatensatz
- uspto-grants-1986_04
- Patentnummer
- US04584397
Notizen zur Reaktion
Wird geladen…