Sulfuric Acid → 4-Prop-2-ynylcyclohexanecarboxylic acid

HRID 1765031Notes

Reaction equation

HRID 1765031 reaction equation
S(=O)(=O)(O)[OH:2].[CH2:6]([CH:9]1[CH2:14][CH2:13][CH:12]([CH2:15][OH:16])[CH2:11][CH2:10]1)[C:7]#[CH:8]>CC(C)=O.CCOCC.[O-2].[O-2].[O-2].[Cr+6]>[CH2:6]([CH:9]1[CH2:14][CH2:13][CH:12]([C:15]([OH:2])=[O:16])[CH2:11][CH2:10]1)[C:7]#[CH:8]

Participants

6

Reactant 2

HCID 1118Sulfuric AcidHCID 10796940(4-Prop-2-ynylcyclohexyl)methanol

Product 1

HCID 107971444-Prop-2-ynylcyclohexanecarboxylic acidYield 75%

Reagents, catalysts & solvents 3

HCID 10219390chromium (VI) trioxideCatalystHCID 180AcetoneSolventHCID 3283Diethyl EtherSolvent

Procedure

A solution of chromium trioxide (1.1 g, 11 mmol) in 1.5 M sulfuric acid (40 mL, 27 mmol) was maintained at 0° C. while 5.3 (0.46 g, 3 mmol) in 80 mL of acetone was added over 2 hours. The reaction was then stirred for an additional 2 hours at room temperature. The reaction mixture was diluted with ether (200 mL) and extracted 2 times with water. The organics were dried with sodium sulfate. The solvent was removed under reduced pressure and the product was purified by chromatography on silica gel column eluting with acetone-dichloromethane (70:30) to give 5.4 (75%). 1H NMR (300 MHz, CDCl3) δ 2.24 (dt, J=3.66, 12.1 Hz, 1H), 2.10 (dd, J=2.7, 6.5 Hz, 2H), 2.04–1.89 (m, 5H), 1.76 (d, J=2.3 Hz, 1H), 1.43 (dq, J=3.28, 13.1 Hz, 2H), 1.03 (dq, J=3.28, 13.1 Hz, 2H). 13C NMR (300 MHz, CDCl3) δ183.2, 83.3, 69.9, 43.4, 36.7, 31.8, 28.9, 26.3.

Workup

  1. additionwas added over 2 hours
  2. extractionextracted 2 times with water
  3. dry with materialThe organics were dried with sodium sulfate
  4. customThe solvent was removed under reduced pressure
  5. customthe product was purified by chromatography on silica gel column
  6. washeluting with acetone-dichloromethane (70:30)

Sources & evidence

ORD record
ord-615b74046ece431cb4885a6b4c24a99a
Source dataset
uspto-grants-2007_06
Patent number
US07226913B2

Reaction notes

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