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Formic Acid → 2,6-Dimethyl-4-hydroxybenzaldehyde

HRID 1274467
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HRID 1274467 반응식
C([O:4][C:5]1[CH:12]=[C:11]([CH3:13])[C:8]([CH:9]=[O:10])=[C:7]([CH3:14])[CH:6]=1)C=C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(O)=O>C(OCC)(=O)C.CC(O)=O.CC(O)=O.[Pd]>[CH3:13][C:11]1[CH:12]=[C:5]([OH:4])[CH:6]=[C:7]([CH3:14])[C:8]=1[CH:9]=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 284Formic AcidHCID 11776TriphenylphosphineHCID 185158104-Allyloxy-2,6-dimethyl-benzaldehyde

생성물 1

HCID 5910722,6-Dimethyl-4-hydroxybenzaldehyde수율 51%

시약·촉매·용매 2

HCID 4144353Palladium (II) acetate촉매HCID 8857Ethyl Acetate
용매

실험 절차

4-Allyloxy-2,6-dimethyl-benzaldehyde, 9.67 g (50.9 mmole), 1.14 g (5.09 mmole) of palladium II acetate, and 8.00 g (30.5 mmole)of triphenylphosphine was mixed in a flask. Formic acid, 2.11 ml (56 mmole), was added and the mixture was swirled in a 800 oil bath. Within 15 seconds the reaction exothermed and turned very dark. The gum was dissolved in ethyl acetate, washed once in sodium bicarbonate, once in water, and once in brine then chromatographed on 350 ml silica, using 20%, then 40% ethyl acetate/hexane. Fractions were bulked and crystallize from methylene chloride/hexane to give 3.90 g (51%) of subtitled product which was used without further purification.

후처리

  1. washwashed once in sodium bicarbonate, once in water
  2. customonce in brine then chromatographed on 350 ml silica
  3. customcrystallize from methylene chloride/hexane

출처 및 근거

ORD 기록
ord-67346c36cace4126b89e57eb71f58709
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06156748

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