Sodium sulfate decahydrate → 3-Chloro-5-(hydroxymethyl)benzamide

HRID 917549Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 917549
[C:1]([C:4]1[CH:5]=[C:6]([CH:11]=[C:12]([Cl:14])[CH:13]=1)[C:7](OC)=[O:8])(=[O:3])[NH2:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+]>C1COCC1>[Cl:14][C:12]1[CH:13]=[C:4]([CH:5]=[C:6]([CH2:7][OH:8])[CH:11]=1)[C:1]([NH2:2])=[O:3]

Komponenten

5

Edukt 3

HCID 62649Sodium sulfate decahydrateHCID 21226445Aluminium lithium hydrideHCID 58963003Methyl 3-carbamoyl-5-chlorobenzoate

Produkt 1

HCID 589629763-Chloro-5-(hydroxymethyl)benzamideAusbeute 40,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Step N4. To above methyl 3-carbamoyl-5-chlorobenzoate (˜9.3 mmol) in dry THF (100 mL) was added lithium aluminum hydride (1 g, 26.3 mmol) in portions. The mixture was stirred for 4 hours, then treated with sodium sulfate decahydrate (8.5 g, 26.3 mmol) for 30 min. The solid was filtered off and washed with THF for three times. The solvent was removed under vacuum and resulting residue was purified by column with DCM, then MeOH/DCM (5/95) to give 3-chloro-5-(hydroxymethyl)benzamide (13, 0.7 g, 40%).

Aufarbeitung

  1. filtrationThe solid was filtered off
  2. washwashed with THF for three times
  3. customThe solvent was removed under vacuum
  4. customresulting residue
  5. customwas purified by column with DCM

Quellen und Nachweise

ORD-Eintrag
ord-34bbf0fd00814662ab934bddc8ca2f90
Quelldatensatz
uspto-grants-2007_09
Patentnummer
US07273882B2

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