Reaktion #55918

ord-e49145092cdf4b1ca864bdd569e42458

Reaktionsgleichung

O
water
[H-].[Na+]
sodium hydride
COc1ccc2c(c1)C(C)(C)CO2
2,3-dihydro-5-methoxy-3,3-dimethylbenzofuran
CCS
ethanethiol
CC1(C)COc2ccc(O)cc21
2,3-dihydro-3,3-dimethyl-benzofuran-5-ol

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturunder reflux in a nitrogen atmosphere for 3 hours
  2. 2
    Waschenthe aqueous phase washed with chloroform
  3. 3
    Extraktionextracted into ether
  4. 4
    SonstigeThe ether was evaporated off

Vorschrift

A solution of ethanethiol (12.6 parts) in dimethyl formamide (60 parts) was added with stirring under nitrogen over a period of 20 minutes to a mixture of sodium hydride (6.6 parts of 80% dispersion in oil) and dry dimethyl formamide (60 parts) cooled to 0° C. After 10 minutes, a solution of 2,3-dihydro-5-methoxy-3,3-dimethylbenzofuran (18 parts) in dimethyl formamide (40 parts) was added and the mixture boiled under reflux in a nitrogen atmosphere for 3 hours. The mixture was then added to water and the aqueous phase washed with chloroform, acidified with hydrochloric acid and extracted into ether. The ether was evaporated off to yield 2,3-dihydro-3,3-dimethyl-benzofuran-5-ol (5.4 parts) as a brown oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04222767uspto-grants-1980_09