1,5-Dibromopentane → HCID 19996099, compound

HRID 1086897Notes

Reaction equation

HRID 1086897 reaction equation
[O:1]1[C:5]([CH2:6][CH2:7][OH:8])=[CH:4][C:3]2[CH:9]=[CH:10][CH:11]=[CH:12][C:2]1=2.[Br:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]Br.[OH-].[Na+]>>[Br:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][O:8][CH2:7][CH2:6][C:5]1[O:1][C:2]2[CH:12]=[CH:11][CH:10]=[CH:9][C:3]=2[CH:4]=1

Participants

4

Procedure

A mixture of 2-benzo(b)furanethanol (2.00 g), 1,5-dibromopentane (6 ml), 50% sodium hydroxide (7 ml) and TAB (0.2 g) was vigorously stirred at 24° for 21 h, then partitioned between water (50 ml) and ether (60 ml). The organic phase was washed with brine (50 ml), dried and evaporated in vacuo. The oily residue was purified by FCC eluting with hexane-diethyl ether (97:3) to give the title compound as a colourless oil (2.70 g), t.l.c. (hexane-diethyl ether 4:1) Rf 0.54.

Workup

  1. custompartitioned between water (50 ml) and ether (60 ml)
  2. washThe organic phase was washed with brine (50 ml)
  3. customdried
  4. customevaporated in vacuo
  5. customThe oily residue was purified by FCC
  6. washeluting with hexane-diethyl ether (97:3)

Sources & evidence

ORD record
ord-d21a055443e443e481af45cdfb38bf5b
Source dataset
uspto-grants-1991_07
Patent number
US05032609

Reaction notes

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