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Isopropanol → (-) Ammonium(4S)-p-menth-1-ene-7-sulfonate

HRID 364857
ノート
印刷プレビュー

反応式

HRID 364857 の反応式
C(O)(C)C.[CH3:5][C:6]1([CH3:14])[CH:12]2[CH2:13][CH:7]1[CH2:8][CH2:9][C:10]2=[CH2:11].[S:15](=[O:18])([OH:17])[O-:16].[NH4+:19]>O>[C:10]1([CH2:11][S:15]([O-:18])(=[O:17])=[O:16])[CH2:12][CH2:13][C@H:7]([CH:6]([CH3:14])[CH3:5])[CH2:8][CH:9]=1.[NH4+:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3776IsopropanolHCID 14896Beta-PineneHCID 10441651Ammonium Bisulfite

生成物 1

HCID 86740958(-) Ammonium(4S)-p-menth-1-ene-7-sulfonate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Into a 1 liter flask equipped with magnetic stirrer were placed 450 ml isopropanol, 240 ml water and 54.4 grams (0.4 mole) β-pinene. Ammonium bisulfite, 105 grams (45%) was then added thereto. The mixture was stirred at 40°-45° C. for 22 hours. Thereafter, the solution was evaporated to dryness. Residue was extracted with methanol. The methanolic solution was filtered, and the resultant filtrate evaporated to dryness. Obtained were 84 grams product (85.8% purity; 77% yield).

後処理

  1. customInto a 1 liter flask equipped with magnetic stirrer
  2. customThereafter, the solution was evaporated to dryness
  3. extractionResidue was extracted with methanol
  4. filtrationThe methanolic solution was filtered
  5. customthe resultant filtrate evaporated to dryness
  6. customObtained

出典と根拠

ORDレコード
ord-67e9e610eb794563b4d1adf68a722109
出典データセット
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04606851

反応ノート

読み込み中…

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