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Dimethyl Sulfoxide → 5-Tert-butylpyridine-3-carbaldehyde

HRID 2071081
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HRID 2071081 반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[C:11]([C:15]1[CH:16]=[C:17]([CH2:21][OH:22])[CH:18]=[N:19][CH:20]=1)([CH3:14])([CH3:13])[CH3:12].C(N(CC)CC)C>C(Cl)Cl>[C:11]([C:15]1[CH:20]=[N:19][CH:18]=[C:17]([CH:16]=1)[CH:21]=[O:22])([CH3:14])([CH3:12])[CH3:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 53779320(5-(tert-Butyl)pyridin-3-yl)methanol

생성물 1

HCID 595699785-Tert-butylpyridine-3-carbaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

Oxalyl chloride (158 μL, 1.819 mmol) in methylene chloride (10 mL) was placed in a two-necked flask at −78° C., followed by the addition of dimethyl sulfoxide (129 μL, 1.819 mmol). Stirring was continued for 20 min, followed by addition of (5-tert-butylpyridin-3-yl)methanol (0.2 g, 1.21 mmol) in methylene chloride (10 mL). After the mixture was stirred at −78° C. for additional 20 min, triethylamine (0.59 mL, 4.24 mmol) was added. The cooling bath was removed and the suspension was allowed to warm to room temperature. Water (50 mL) was added, the yellow organic layer was separated, and the aqueous layer was extracted with methylene chloride (3×30 mL). The combined organic solution was dried and concentrated to give 5-tert-butylnicotinaldehyde as an orange-yellow liquid which was used directly for next step without further purification.

후처리

  1. stirringAfter the mixture was stirred at −78° C. for additional 20 min
  2. customThe cooling bath was removed
  3. additionWater (50 mL) was added
  4. customthe yellow organic layer was separated
  5. extractionthe aqueous layer was extracted with methylene chloride (3×30 mL)
  6. customThe combined organic solution was dried
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c057b322682f44368de96eb2ed4d5f3f
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299267B2

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