Diiodomethane → 4-Bromo-1-chloro-2-(4-(cyclopropoxymethyl)benzyl)benzene

HRID 2038521노트

반응식

HRID 2038521 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[C:4]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][O:17][CH:18]=[CH2:19])=[CH:12][CH:11]=2)[CH:3]=1.[Zn](CC)[CH2:21]C.ICI>C(OCC)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[C:4]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([CH2:16][O:17][CH:18]3[CH2:21][CH2:19]3)=[CH:12][CH:11]=2)[CH:3]=1

참가 물질

5

실험 절차

To a stirred mixture of 4-bromo-1-chloro-2-(4-(vinyloxymethyl)benzyl)benzene (0.7 g, 2.07 mmol) and Et2Zn (5.18 mL, 5.18 mmol, 1.0 M in hexane) in dry ethyl ether (10 mL) was added diiodomethane (0.42 mL, 5.18 mmol) dropwise during 20 min at room temperature under argon. After stirring overnight, the reaction mixture was poured slowly into ice cold dilute hydrochloride solution with stirring. The mixture was extracted with ethyl acetate (3×20 mL). The combined organic layers were washed with water (20 mL) and then with brine (20 mL), and then dried over sodium sulfate. The residue was concentrated and purified by column chromatography (eluent EA:PE=1:200) to obtain intermediate CV (0.6 g) as a colorless oil. 1H NMR (CDCl3, 400 MHz): δ 7.33˜7.24 (m, 5H), 7.18 (d, 2H), 4.55 (s, 2H), 4.07 (s, 2H), 3.40˜3.37 (m, 1H), 0.69˜0.49 (m, 4H).

후처리

  1. additionthe reaction mixture was poured slowly into ice cold dilute hydrochloride solution
  2. stirringwith stirring
  3. extractionThe mixture was extracted with ethyl acetate (3×20 mL)
  4. washThe combined organic layers were washed with water (20 mL)
  5. dry with materialwith brine (20 mL), and then dried over sodium sulfate
  6. concentrationThe residue was concentrated
  7. custompurified by column chromatography (eluent EA:PE=1:200)
  8. customto obtain intermediate CV (0.6 g) as a colorless oil

출처 및 근거

ORD 기록
ord-d16991501e754c86808dcc151aba88c7
출처 데이터셋
uspto-grants-2013_11
특허 번호
US08575321B2

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