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Water → 7-bromo-5-fluoro-3,4-dihydro-2H-naphthalen-1-ol

HRID 2089482
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HRID 2089482 반응식
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][C:9]2=[O:12])=[C:4]([F:13])[CH:3]=1.[BH4-].[Na+].O>CO.ClCCl>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][CH:9]2[OH:12])=[C:4]([F:13])[CH:3]=1
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참가 물질

6

반응물 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 591994027-Bromo-5-fluoro-3,4-dihydronaphthalen-1(2H)-one

생성물 1

HCID 675473967-bromo-5-fluoro-3,4-dihydro-2H-naphthalen-1-ol

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

To a solution of 7-bromo-5-fluoro-3,4-dihydro-2H-naphthalen-1-one (0.290 g, 1.145 mmol) in methanol (8 mL) and dichloromethane (2 mL) at 0° C. is added sodium borohydride (0.066 g, 1.718 mmol) in one portion. After 2 hours at 0° C., water (30 mL) is added and the volatile organics are removed in vacuo. The resulting mixture is extracted with dichloromethane, dried over magnesium sulfate, filtered, and concentrated to afford 7-bromo-5-fluoro-3,4-dihydro-2H-naphthalen-1-ol, which is used in the next step without further purification.

후처리

  1. customthe volatile organics are removed in vacuo
  2. extractionThe resulting mixture is extracted with dichloromethane
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-dd8bc7b5dc99437a8450a26b02791df5
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08436035B2

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