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Water → 1-[Bromo(phenyl)methyl]naphthalene

HRID 41324
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HRID 41324 반응식
[C:1]1([CH:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.P(Br)(Br)[Br:20].O>C(OCC)C>[Br:20][CH:11]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 24614Phosphorus tribromideHCID 226163Naphthalen-1-yl(phenyl)methanol

생성물 1

HCID 582386271-[Bromo(phenyl)methyl]naphthalene수율 138.5%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a solution of 32.3 g (138 mmol) of 7 in 150 mL of dry diethyl ether, 24.8 g (8.62 mL, 91.6 mmol) of PBr3 was added at −10° C. The resulting mixture was stirred for 12 hr at room temperature and then added to 450 mL of cold water. The organic layer was separated, and the aqueous layer was extracted with 2×150 mL of water. The combined organic extracts were washed with aqueous NaHCO3, dried over Na2SO4, and then evaporated to dryness. This procedure gave 37.7 g (92%) of 8.

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후처리

  1. customThe organic layer was separated
  2. extractionthe aqueous layer was extracted with 2×150 mL of water
  3. washThe combined organic extracts were washed with aqueous NaHCO3
  4. dry with materialdried over Na2SO4
  5. customevaporated to dryness

출처 및 근거

ORD 기록
ord-803a1df4ba5f4e028f869e71911b3ae9
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08530593B2

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