Water → HCID 11702831, compound

HRID 750775Notes

Reaction equation

HRID 750775 reaction equation
O[Li].O.O.C([O:7][C:8]([C:10]1([CH2:14][CH2:15][CH2:16][CH2:17][C:18](=[O:32])[CH2:19][CH2:20][CH2:21][CH2:22][C:23]2([C:27]([O:29]CC)=[O:28])[CH2:26][CH2:25][CH2:24]2)[CH2:13][CH2:12][CH2:11]1)=[O:9])C>CCO>[C:27]([C:23]1([CH2:22][CH2:21][CH2:20][CH2:19][C:18](=[O:32])[CH2:17][CH2:16][CH2:15][CH2:14][C:10]2([C:8]([OH:9])=[O:7])[CH2:11][CH2:12][CH2:13]2)[CH2:26][CH2:25][CH2:24]1)([OH:29])=[O:28]

Participants

5

Reactant 3

HCID 962WaterHCID 168937Lithium hydroxide, monohydrateHCID 21069430HCID 21069430, compound

Product 1

HCID 11702831HCID 11702831, compoundYield 56%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

LiOH·H2O (3.94 g, 93.9 mmol) and H2O (30 mL) were added to a solution of ethyl 1-9-[1-(ethoxycarbonyl)cyclobutyl]-5-oxononyl-1-cyclobutanecarboxylate (9.20 g, 23.3 mmol) in EtOH (90 mL) and the resulting mixture was stirred at reflux temperature for 17 h, allowed to cool to rt and concentrated in vacuo to a smaller volume. H2O (150 mL) was added and the resulting mixture was extracted with Et2O (50 mL), acidified with aqueous HCl (6 M, 25 mL) and extracted with Et2O (1×100 mL, 2×50 mL). The latter organic layers were combined, washed with brine (50 mL), dried (Na2SO4) and evaporated in vacuo. The remaining residue was recrystallized from a mixture of iPr2O and heptane to give 1-[9-(1-carboxycyclobutyl)-5-oxononyl]-1-cyclo-butanecarboxylic acid (4.41 g, 56%) as small, white granules. mp 69-70° C. 1H NMR (CDCl3): δ=11.2 (br s, 2H), 2.50-2.37 (m, 4H), 2.39 (t, J=7.2 Hz, 4H), 1.96-1.84 (m, 8H), 1.81-1.75 (m, 4H), 1.57 (quintet, J=7.4 Hz, 4H), 1.26-1.12 (m, 4H). 13C NMR (CDCl3): δ=210.6, 183.4 (2×), 47.6 (2×), 42.7 (2×), 37.8 (2×), 30.1 (4×). 24.7 (2×), 24.1 (2×), 15.7 (2×). Anal. calcd for C19H30O5: C, 67.43; H, 8.93; found: C, 67.19; H, 8.97.

Workup

  1. temperatureat reflux temperature for 17 h
  2. concentrationconcentrated in vacuo to a smaller volume
  3. additionH2O (150 mL) was added
  4. extractionthe resulting mixture was extracted with Et2O (50 mL)
  5. extractionextracted with Et2O (1×100 mL, 2×50 mL)
  6. washwashed with brine (50 mL)
  7. dry with materialdried (Na2SO4)
  8. customevaporated in vacuo
  9. customThe remaining residue was recrystallized from a mixture of iPr2O and heptane

Sources & evidence

ORD record
ord-35f5e8dcfa2b4e42a4a6a4e8d684b493
Source dataset
uspto-grants-2008_07
Patent number
US07405226B2

Reaction notes

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