tert-Butyl acetate → rac-(1R*,8R*,9R*)-(9-hydroxy-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-yl)-acetic acid tert-butyl ester

HRID 1879348

반응식

HRID 1879348 반응식
C([Li])CCC.[C:6]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])(=[O:8])[CH3:7].[CH:14]12[CH2:26][CH2:25][CH:21]([C:22](=[O:24])[CH2:23]1)[C:20]1[C:15]2=[CH:16][CH:17]=[CH:18][CH:19]=1>C1COCC1.C1(C)C=CC=CC=1>[C:10]([O:9][C:6](=[O:8])[CH2:7][C:22]1([OH:24])[CH2:23][CH:14]2[CH2:26][CH2:25][CH:21]1[C:20]1[C:15]2=[CH:16][CH:17]=[CH:18][CH:19]=1)([CH3:13])([CH3:12])[CH3:11]

참가 물질

6

반응물 3

HCID 10908tert-Butyl acetateHCID 5825961,4-Ethanonaphthalen-2(1H)-one, 3,4-dihydro-HCID 178418339Butyllithium

생성물 1

HCID 70999528rac-(1R*,8R*,9R*)-(9-hydroxy-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-yl)-acetic acid tert-butyl ester

시약·촉매·용매 2

HCID 1140Toluene용매2회HCID 8028Tetrahydrofuran용매

반응 조건

온도
-50 °C

실험 절차

To a solution of 3.5 mL of DIPA in 6 mL THF were added dropwise 9.9 mL of n-butyllithium (2.5M in Hept) at −20° C. After 20 min, 12 mL of toluene were added and the solution was stirred for 30 min. The mixture was cooled to −50° C., 4.5 mL of tert.-butyl acetate were added and stirring was continued for 1 h at −50° C. Then, 2.5 g of rac-(1R*,8R*)-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-one dissolved in 6 mL of toluol were added and the solution was stirred at −50 to −20° C. over 2.5 h. The reaction mixture was poured on ice/aq. HCl, the organic phase was separated, washed with sat. aq. NaHCO3, dried over Na2SO4 and concentrated in vacuo. The crude reaction product was purified by CC with Hept/EtOAc (4:1) to yield 2.6 g of the major racemate, rac-(1R*,8R*,9R*)-(9-hydroxy-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-yl)-acetic acid tert-butyl ester as beige solid and 0.4 g of the minor racemate, rac-(1R*,8R*,9S*)-(9-hydroxy-tricyclo[6.2.2.02,7]dodeca-2,4,6-trien-9-yl)-acetic acid tert-butyl ester as yellow oil.

후처리

  1. stirringstirring
  2. waitwas continued for 1 h at −50° C
  3. additionwere added
  4. stirringthe solution was stirred at −50 to −20° C. over 2.5 h
  5. additionThe reaction mixture was poured on ice/aq
  6. customHCl, the organic phase was separated
  7. washwashed with sat. aq. NaHCO3
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated in vacuo
  10. customThe crude reaction product
  11. customwas purified by CC with Hept/EtOAc (4:1)

출처 및 근거

ORD 기록
ord-f56bf62e87d2453aaf7d19ff1b74c014
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08314253B2

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