Water → 2-((2-((6-Bromohexyl)oxy)ethoxy)methyl)-1,3-dichlorobenzene

HRID 2369712Notes

Reaction equation

HRID 2369712 reaction equation
[OH-].[Na+].[Cl:3][C:4]1[CH:14]=[CH:13][CH:12]=[C:11]([Cl:15])[C:5]=1[CH2:6][O:7][CH2:8][CH2:9][OH:10].[Br:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]Br.O>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[Br:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][O:10][CH2:9][CH2:8][O:7][CH2:6][C:5]1[C:4]([Cl:3])=[CH:14][CH:13]=[CH:12][C:11]=1[Cl:15]

Participants

7

Procedure

50% aq NaOH (1.89 L), 2-(2,6-dichlorobenzyloxy)ethanol (473.2 g), 1,6-dibromohexane (2.44 kg, 5 eq) and tetrabutylammonium bromide (34.1 g, 5 mol %) in toluene (1.89 L) was heated to 55-60° C. for 8-20 h. On cooling water (558 mL) and toluene (558 mL) were added. The aqueous phase was separated and diluted with water (1 L) then back extracted with toluene (1.1 L). The combined toluene extracts were washed twice with water (2.2 L), then evaporated to dryness on a rotary evaporator. The excess 1,6-dibromohexane was removed using a wiped film evaporator, and the resulting crude product chromatographed on silica (5 kg Biotage), eluting with 5% ethyl acetate in petrol 60/80, to give the title compound (503.2 g)—LC RT=7.0 min.

Workup

  1. additionwere added
  2. customThe aqueous phase was separated
  3. additiondiluted with water (1 L)
  4. extractionthen back extracted with toluene (1.1 L)
  5. washThe combined toluene extracts were washed twice with water (2.2 L)
  6. customevaporated to dryness on a rotary evaporator
  7. customThe excess 1,6-dibromohexane was removed
  8. customa wiped film evaporator
  9. customthe resulting crude product chromatographed on silica (5 kg Biotage)
  10. washeluting with 5% ethyl acetate in petrol 60/80

Sources & evidence

ORD record
ord-17b40fbeb8b042e4aee036af3b27fc93
Source dataset
uspto-grants-2014_04
Patent number
USRE044874E1

Reaction notes

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