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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Toluenesulfonyl chloride → 2,5-Difluoro-3-methoxyphenylacetonitrile

HRID 1108096
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HRID 1108096 반응식
[F:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][C:7]([F:12])=[CH:6][C:3]=1[CH2:4]O.C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[CH2:24]([N:26](CC)CC)C.[C-]#N.[Na+]>ClCCl.O.CS(C)=O>[F:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][C:7]([F:12])=[CH:6][C:3]=1[CH2:4][C:24]#[N:26]
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참가 물질

8

반응물 4

HCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 8929Sodium CyanideHCID 114466172,5-Difluoro-3-methoxybenzyl alcohol

생성물 1

HCID 114353352,5-Difluoro-3-methoxyphenylacetonitrile수율 68.1%

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide
용매
HCID 962Water용매2회
HCID 6344Dichloromethane용매

실험 절차

To a stirred solution of 2,5-difluoro-3-methoxybenzyl alcohol (8.26 g, 47.4 mmol) in dichloromethane (100 ml) was added p-toluenesulfonyl chloride (9.95 g, 52.2 mmol) and triethylamine (7.30 ml, 52.2 mmol) at room temperature. After 3.5 hr, the mixture was poured into water (200 ml) and extracted with ether (200 ml). The extract was washed with brine (200 ml), dried (magnesium sulfate) and evaporated. To the residue was added DMSO (200 ml) and sodium cyanide (3.48 g, 71 mmol). The resulting mixture was stirred for 2 hr and then poured into water (200 ml) and extracted with ether (300 ml). The extract was washed with water (100 ml), brine (100 ml) and dried over magnesium sulfate. Removal of solvent gave 5.91 g (63%) of the titled compound as a red oil.

후처리

  1. extractionextracted with ether (200 ml)
  2. washThe extract was washed with brine (200 ml)
  3. dry with materialdried (magnesium sulfate)
  4. customevaporated
  5. extractionextracted with ether (300 ml)
  6. washThe extract was washed with water (100 ml), brine (100 ml)
  7. dry with materialdried over magnesium sulfate
  8. customRemoval of solvent

출처 및 근거

ORD 기록
ord-eb8491a188fe43cd95e764be17c905ab
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06063928

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