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Dimethyl Sulfoxide → 2,5-Dichloro-4-fluorobenzaldehyde

HRID 849260
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HRID 849260 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[Cl:11][C:12]1[CH:19]=[C:18]([F:20])[C:17]([Cl:21])=[CH:16][C:13]=1[CH2:14][OH:15].C(N(CC)CC)C>C(Cl)Cl>[Cl:11][C:12]1[CH:19]=[C:18]([F:20])[C:17]([Cl:21])=[CH:16][C:13]=1[CH:14]=[O:15]
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참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 54012777HCID 54012777, 화합물

생성물 1

HCID 193699312,5-Dichloro-4-fluorobenzaldehyde수율 97.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

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온도
-78 °C

실험 절차

To a solution of oxalyl chloride (1.72 mL, 19.74 mmol) in 20 mL methylene chloride at -78° C. was added a solution DMSO (2.8 mL, 39.5 mL) in 3 mL methylene chloride. The mixture was stirred for 5 minutes at -78° C. followed by the addition of a solution of Part A 2,5-dichloro-4-fluorobenzyl alcohol (3.5 g, 17.95 mmol) from above in 15 mL methylene chloride. The mixture was stirred at -40° C. for 15 min., cooled to -78° C. followed by the addition of triethylamine (8.26 mL, 59.2 mmol). The mixture was allowed to come to RT, washed sequentially with 10% HCl, saturated sodium bicarbonate solution and water. The organic layer was dried over magnesium sulfate and concentrated to afford the title compound 3.39 g as a white solid. ##STR266##

후처리

  1. stirringThe mixture was stirred at -40° C. for 15 min.
  2. temperaturecooled to -78° C.
  3. customto come to RT
  4. washwashed sequentially with 10% HCl, saturated sodium bicarbonate solution and water
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-d1a14156b1044f72ae53ac7adeac2694
출처 데이터셋
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06011059

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