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Hydrochloric Acid → 2-Amino-3-cycloheptylpropanoic acid

HRID 1018847
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HRID 1018847 반응식
C([O:5][C:6](=[O:30])[CH:7]([N:16]=C(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:8][CH:9]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)(C)(C)C.Cl>CO>[NH2:16][CH:7]([CH2:8][CH:9]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1)[C:6]([OH:30])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 865853992-(Benzhydrylidene-amino)-3-cycloheptyl-propionic acid tert-butyl ester

생성물 1

HCID 221843862-Amino-3-cycloheptylpropanoic acid수율 53.7%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 2-(Benzhydrylidene-amino)-3-cycloheptyl-propionic acid tert-butyl ester (1.34 g; 3.31 mmol) in methanol (5 mL) was added 10N HCl solution (15 mL) and the mixture heated to reflux. After 15 h, the mixture was allowed to cool to room temperature and transferred to a separatory funnel and washed with ethyl acetate. The aqueous layer was then neutralized with concentrated ammonium hydroxide solution and the white solid was filtered off and air dried to give 329 mg of 2-Amino-3-cycloheptyl-propionic acid.

후처리

  1. temperaturethe mixture heated to reflux
  2. customtransferred to a separatory funnel
  3. washwashed with ethyl acetate
  4. filtrationthe white solid was filtered off
  5. customair dried

출처 및 근거

ORD 기록
ord-91989a8bdd7242319ae9b2738ae692c3
출처 데이터셋
uspto-grants-2002_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06482951B2

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