3-(2-Bromoethyl)phenol → HCID 68872917、化合物

HRID 2112035ノート

反応式

HRID 2112035 の反応式
[Br:1][CH2:2][CH2:3][C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1>C(Cl)Cl>[Br:1][CH2:2][CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][C:4]([CH3:5])([CH3:9])[CH3:3])[CH:5]=1

参加物

3

実験手順

3-(2-Bromoethyl)phenol (1.349 g, 6.709 mmol) in DCM (7 ml) was cooled under argon to −78° C. Under stirring, isobutene was bubbled into the mixture until more than 5 ml were added. Trifluoromethanesulphonic acid (50 μl) was dropped in. The mixture was stirred under argon at −78° C. for 4.5 hours. Triethylamine (120 μl) was added. The reaction mixture was allowed up to room temperature and then filtered. The filtrate was evaporated to dryness and petroleum ether (25 ml) was added into the residue. It was then filtered and evaporated. The obtained oil was solved in ethyl acetate, washed with water, dried (sodium sulphate) and evaporated. The residue was dissolved in CDCl3 and then evaporated. 1.223 g desired product was left, yield 71%.

後処理

  1. customisobutene was bubbled into the mixture until more than 5 ml
  2. additionwere added
  3. additionTrifluoromethanesulphonic acid (50 μl) was dropped in
  4. stirringThe mixture was stirred under argon at −78° C. for 4.5 hours
  5. additionTriethylamine (120 μl) was added
  6. customwas allowed up to room temperature
  7. filtrationfiltered
  8. customThe filtrate was evaporated to dryness and petroleum ether (25 ml)
  9. additionwas added into the residue
  10. filtrationIt was then filtered
  11. customevaporated
  12. washwashed with water
  13. dry with materialdried (sodium sulphate)
  14. customevaporated
  15. dissolutionThe residue was dissolved in CDCl3
  16. customevaporated
  17. wait1.223 g desired product was left

出典と根拠

ORDレコード
ord-dc53290d06f443b0b1787b9613f7fb1e
出典データセット
uspto-grants-2009_04
特許番号
US07521461B2

反応ノート

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