tert-Butanol → HCID 54447207, compound

HRID 1111409Notes

Reaction equation

HRID 1111409 reaction equation
Br[C:2]1[O:6][C:5]([C:7]([OH:9])=[O:8])=[CH:4][CH:3]=1.[CH2:10]([OH:26])[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH:18]=[CH:19][CH2:20][CH:21]=[CH:22][CH2:23][CH:24]=[CH2:25].CC(C)([O-])C.[K+].C(O)(C)(C)C>C1(C)C=CC=CC=1>[CH2:10]([O:26][C:2]1[O:6][C:5]([C:7]([OH:9])=[O:8])=[CH:4][CH:3]=1)[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH:18]=[CH:19][CH2:20][CH:21]=[CH:22][CH2:23][CH:24]=[CH2:25]

Participants

6

Conditions

Temperature
110 °C

Procedure

A mixture of 57.0 g (0.300 mole) of 5-bromo-2-furoic acid, 119.0 (0.450 mole) of 9,12,15-hexadecatrienol, and 84 g (0.750 mole) of potassium tert-butoxide in dry toluene is stirred with heating. The tert-butanol formed in the reaction is allowed to distill off, and the mixture is refluxed at 110° C. with stirring from 48 hours. The mixture is allowed to cool, then is acidified with acetic acid and diluted with ice water. The toluene organic layer is separated, washed with water, then extracted three times with 5% sodium bicarbonate solution. The combined aqueous extracts are cooled and acidified with 10% HCl solution to give 5-(9,12,15-hexadecatrienyloxy)-2-furoic acid.

Workup

  1. temperaturewith heating
  2. distillationto distill off
  3. stirringwith stirring from 48 hours
  4. temperatureto cool
  5. additiondiluted with ice water
  6. customThe toluene organic layer is separated
  7. washwashed with water
  8. extractionextracted three times with 5% sodium bicarbonate solution
  9. temperatureThe combined aqueous extracts are cooled

Sources & evidence

ORD record
ord-49023382e0d24d75b8be25ab4a6aabd7
Source dataset
uspto-grants-1990_12
Patent number
US04980371

Reaction notes

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