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Boron tribromide → HCID 58415368, 화합물

HRID 2075228
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HRID 2075228 반응식
B(Br)(Br)Br.[I:5][C:6]1[CH:7]=[C:8]([CH:16]=[CH:17][C:18]=1[O:19]C)[CH2:9][C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=1>C(Cl)Cl>[I:5][C:6]1[CH:7]=[C:8]([CH2:9][C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[CH:16]=[CH:17][C:18]=1[OH:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 58415249HCID 58415249, 화합물

생성물 1

HCID 58415368HCID 58415368, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Boron tribromide (11.1 mL, 11.1 mmol, 1M in DCM) was added to a solution of 3-(3-iodo-4-methoxybenzyl)pyridine (720 mg, 2.21 mmol) in DCM (3 mL) at 0° C., and the mixture was stirred for 1 h. The mixture was quenched by the careful addition of water, the layers were separated, and the organic layer was washed with water three times. The combined organic extracts were dried over MgSO4, concentrated in vacuo, and purified by column chromatography to give 2-iodo-4-(pyridin-3-ylmethyl)phenol as a yellow oil. MS (ESI) m/z: Calculated: 311.0; Observed: 312.3 (M++1).

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  1. customThe mixture was quenched by the careful addition of water
  2. customthe layers were separated
  3. washthe organic layer was washed with water three times
  4. dry with materialThe combined organic extracts were dried over MgSO4
  5. concentrationconcentrated in vacuo
  6. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-5364a949198f4dab9ecd3f4d4555dc9a
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07919519B2

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