홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Potassium tert-butoxide → HCID 86700852, 화합물

HRID 881749
노트
인쇄 미리보기

반응식

HRID 881749 반응식
[Cl-].[CH3:2][O:3][CH3:4].[C:5]1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(C)([O-])C.[K+].[Br:30][CH:31]1[C:36]2([C:39]3[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][CH:40]=3)[CH2:37][CH2:38][C:33](C=O)([CH2:34][O:35]2)[CH2:32]1>O1CCCC1>[Br:30][CH:31]1[C:36]2([C:39]3[CH:44]=[CH:43][C:42]([Cl:45])=[CH:41][CH:40]=3)[CH2:37][CH2:38][C:33]([CH:5]=[CH:2][O:3][CH3:4])([CH2:34][O:35]2)[CH2:32]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 23665647Potassium tert-butoxideHCID 86700850HCID 86700850, 화합물HCID 86700853HCID 86700853, 화합물

생성물 1

HCID 86700852HCID 86700852, 화합물수율 95%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of triphenylphosphine methoxymethane chloride (3.51 g, 10.24 mmol) in tetrahydrofuran (20 ml) under nitrogen at room temperature, was added potassium t-butoxide (1.149 g, 10.24 mmol). The reddish solution was stirred at room temperature for 90 minutes. Then a solution of 6-bromo-1-(4-chloro-phenyl)-2-oxa-bicyclo[2.2.2]octane-4-carbaldehyde (2.25 g, 6.83 mmol) in tetrahydrofuran (6 ml) was added to the reaction mixture. The reaction mixture was stirred at room temperature for 10 minutes and then quenched with water (2 ml). The mixture was partitioned between brine (15 ml) and ethyl acetate (60 ml). The aqueous layer was extracted with ethyl acetate (2×30 ml) and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated. The residue was purified by flash chromatography (heptanes/acetone 2/1) to afford the cis and trans mixtures of 6-bromo-1-(4-chloro-phenyl)-4-(2-methoxy-vinyl)-2-oxa-bicyclo[2.2.2]octane (2.32 g, 95%) as colorless oil. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.74-2.99 (m, 6H) 3.54 (3.89 (m, 4H) 3.91-6.36 (m, 5H) 7.28-7.43 (m, 4H).

후처리

  1. stirringThe reaction mixture was stirred at room temperature for 10 minutes
  2. customquenched with water (2 ml)
  3. customThe mixture was partitioned between brine (15 ml) and ethyl acetate (60 ml)
  4. extractionThe aqueous layer was extracted with ethyl acetate (2×30 ml)
  5. washthe combined organic extracts were washed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe residue was purified by flash chromatography (heptanes/acetone 2/1)

출처 및 근거

ORD 기록
ord-42920343c21b4535bc1decb24c3dacf7
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993619B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트