Potassium Hydroxide → HCID 10018662, compound

HRID 1159705Notes

Reaction equation

HRID 1159705 reaction equation
[OH-].[K+].C([O:5][C:6](=[O:28])[C:7]([CH3:27])([CH3:26])[CH2:8][CH2:9][CH2:10][CH2:11][CH:12]([OH:25])[CH2:13][CH2:14][CH2:15][CH2:16][C:17]([CH3:24])([CH3:23])[C:18]([O:20]CC)=[O:19])C>O.C(O)C>[OH:25][CH:12]([CH2:13][CH2:14][CH2:15][CH2:16][C:17]([CH3:24])([CH3:23])[C:18]([OH:20])=[O:19])[CH2:11][CH2:10][CH2:9][CH2:8][C:7]([CH3:27])([CH3:26])[C:6]([OH:28])=[O:5]

Participants

5

Procedure

To a homogeneous solution of potassium hydroxide (3.45 g, 61 mmol) in water (3.3 mL) and ethanol (11.1 mL) was added 7-hydroxy-2,2,12,12-tetramethyltridecanedioic acid diethyl ester (8.2 g, 22 mmol) and the mixture was heated at reflux for 4 h. The mixture was concentrated in vacuo and the residue was extracted with diethyl ether (3×50 mL). The water layer was acidified with concentrated hydrochloric acid (6 mL) to pH 1. The product was extracted with diethyl ether (3′ 100 mL). The combined organic layers were dried over sodium sulfate and concentrated in vacuo. The crude product was purified by column chromatography (silica, dichloromethane:methanol=90:10) to give the pure product (6.6 g, 95%) as a colorless oil. 1H NMR (300 MHz, CDCl3/TMS): δ (ppm): 8.10 (br., 3 H), 3.58 (br., 1 H), 1.62-1.22 (m, 16 H), 1.18 (s, 12 H). 13C NMR (75 MHz, CDCl3/TMS): δ (ppm): 184.3, 71.8, 42.1, 40.5, 36.9, 25.9, 25.0, 24.9. HRMS (LSIMS, gly): Calcd. for C17H33O5 (MH+): 317.2328; found 317.2330. HPLC: 90.4% purity.

Workup

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 4 h
  3. concentrationThe mixture was concentrated in vacuo
  4. extractionthe residue was extracted with diethyl ether (3×50 mL)
  5. extractionThe product was extracted with diethyl ether (3′ 100 mL)
  6. dry with materialThe combined organic layers were dried over sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe crude product was purified by column chromatography (silica, dichloromethane:methanol=90:10)

Sources & evidence

ORD record
ord-4aa76a81d6ae42cfa69a388545653844
Source dataset
uspto-grants-2010_10
Patent number
US07812199B2

Reaction notes

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