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N-bromobutanimide → 7-Bromo-6-hydroxy-1-heptanol

HRID 1263272
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1263272
[CH2:1]([OH:8])[CH2:2][CH2:3][CH2:4]CC=C.[Br:9]N1C(=O)CCC1=O.[C:17]([OH:21])(C)([CH3:19])[CH3:18].O>>[Br:9][CH2:18][CH:17]([OH:21])[CH2:19][CH2:4][CH2:3][CH2:2][CH2:1][OH:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 67184N-bromobutanimide3×HCID 543123Hept-6-en-1-olHCID 714019492-Methylpropan-2-ol--water (1/1)

Produkt 1

HCID 133660747-Bromo-6-hydroxy-1-heptanol

Versuchsvorschrift

To a solution of 3 (500 mg, 4.38 mmol) in t-butanol-water (24 mL-4 mL) in the dark was added N-bromosuccinimide (NBS) (858 mg, 4.82 mmol) in small portions. Additional NBS (312 mg) was added after 4 hours and 16 hours later another 400 mg of NBS was added. The reaction mixture was stirred for 68 hours. After removal of t-butanol in vacuo, the residue was diluted with ether, washed with saturated sodium thiosulfite solution, saturated sodium chloride solution, and dried over magnesium sulfate. The crude product was purified by HPLC to give 123 mg of 7-bromo-6-hydroxy-1-heptanol (4).

Aufarbeitung

  1. additionwas added
  2. customAfter removal of t-butanol in vacuo
  3. additionthe residue was diluted with ether
  4. washwashed with saturated sodium thiosulfite solution, saturated sodium chloride solution
  5. dry with materialdried over magnesium sulfate
  6. customThe crude product was purified by HPLC

Quellen und Nachweise

ORD-Eintrag
ord-ba6d27e779a340eda1b70c0430433cb5
Quelldatensatz
uspto-grants-1984_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04456613

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