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Triphenylphosphine → 2-Nitro-4-(trifluoromethyl)benzaldehyde

HRID 342991
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HRID 342991 반응식
[N+:1]([C:4]1[CH:12]=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:10]=[CH:9][C:5]=1[C:6](Cl)=[O:7])([O-:3])=[O:2].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>CC(C)=O>[N+:1]([C:4]1[CH:12]=[C:11]([C:13]([F:14])([F:15])[F:16])[CH:10]=[CH:9][C:5]=1[CH:6]=[O:7])([O-:3])=[O:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 11776TriphenylphosphineHCID 143235242-Nitro-4-(trifluoromethyl)benzoyl chloride

생성물 1

HCID 111603052-Nitro-4-(trifluoromethyl)benzaldehyde수율 85.5%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A mixture of 2-nitro-4-trifluoromethylbenzoyl chloride (8.0 g) and triphenylphosphine (16.5 g) in dry acetone (75 ml) was treated with bis-(triphenylphosphine)tetrahydroboratocopper(I) (19.8 g). The resulting suspension was stirred for 1 hour, filtered and washed with diethyl ether. The filtrate was evaporated to dryness and the resulting residue was subjected to chromatography, eluting with a mixture of diethyl ether and n-hexane (1:5 v/v), to give 2-nitro-4-trifluoromethylbenzaldehyde (5.91 g) in the form of an off-white solid, m.p. 63° C.

후처리

  1. filtrationfiltered
  2. washwashed with diethyl ether
  3. customThe filtrate was evaporated to dryness
  4. washeluting with a mixture of diethyl ether and n-hexane (1:5 v/v)

출처 및 근거

ORD 기록
ord-a7d09b84d7a7454baf296fa74ae8f382
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859283

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