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

HRID 364857
노트
인쇄 미리보기

반응식

HRID 364857 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 14896Beta-PineneHCID 10441651Ammonium Bisulfite

생성물 1

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

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-67e9e610eb794563b4d1adf68a722109
출처 데이터셋
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04606851

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