Sulfuric Acid → HCID 14347488、化合物

HRID 1110474

反応式

HRID 1110474 の反応式
[CH3:1][CH:2]([CH3:12])[CH2:3][CH:4]=[CH:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1.[N+:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=1[CH2:22][C:23]#[N:24])([O-:15])=[O:14].S(=O)(=O)(O)[OH:26]>C(O)(=O)C>[CH3:1][C:2]([NH:24][C:23](=[O:26])[CH2:22][C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][C:16]=1[N+:13]([O-:15])=[O:14])([CH3:12])[CH2:3][CH2:4][CH2:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1

参加物

5

反応物 3

HCID 1118Sulfuric AcidHCID 118882-NitrophenylacetonitrileHCID 54005742HCID 54005742、化合物

生成物 1

HCID 14347488HCID 14347488、化合物

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A mixture of 22.7 g of 3-(4-methyl-pentenyl)pyridine and 22.8 g of 2-nitrobenzeneacetonitrile in 80 mL of acetic acid was cooled to 12°-13° C. and then 16 mL of sulfuric acid was added dropwise over 6 minutes. The reaction was stirred for 2 hours at ambient temperature, then after the acetic acid was removed in vacuo, 1L of water was added and the mixture was extracted with dichloromethane to remove neutral impurities. The aqueous layer was basified with 10N sodium hydroxide, and extracted with dichloromethane (4×200 mL). The dried (K2CO3) extracts were evaporated to give 35.6 g of N-[1,1-dimethyl-(3-pyridyl)butyl]-2-nitrobenzeneacetamide. A portion was crystallized from ethyl acetate-hexane to yield the analytical sample, mp 117°-118.5° C.

後処理

  1. temperaturewas cooled to 12°-13° C.
  2. customafter the acetic acid was removed in vacuo, 1L of water
  3. additionwas added
  4. extractionthe mixture was extracted with dichloromethane
  5. customto remove neutral impurities
  6. extractionextracted with dichloromethane (4×200 mL)
  7. dry with materialThe dried (K2CO3) extracts
  8. customwere evaporated

出典と根拠

ORDレコード
ord-1c14738cd54e4b118b6f1926139d8fe5
出典データセット
uspto-grants-1990_12
特許番号
US04975438

関連ノート

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