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Hydrochloric Acid → Hydrochloric Acid

HRID 1379629
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HRID 1379629 반응식
C(OC([NH:8][C@H:9]([CH3:18])[CH2:10][O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=O)(C)(C)C.[ClH:19]>C(OCC)(=O)C>[O:11]([CH2:10][C@H:9]([NH2:8])[CH3:18])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[ClH:19]
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 10586857(R)-N-Boc-1-phenoxy-2-propanamine

생성물 2

HCID 313Hydrochloric Acid수율 69%HCID 5324633(2R)-1-Phenoxy-2-propanamine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

실험 절차

(R)- N-(tert-Butoxycarbonyl)-1-phenoxy-2-propylamine (8.0 g, 33 mmol) was dissolved in ethyl acetate (100 ml). A solution of hydrochloric acid (g) in ethyl acetate (6N, 100 ml) was added dropwise at room temperature. The reaction mixture was stirred at room temperature for 20 h during which time a heavy precipitate was formed. The reaction mixture was concentrated to half the original volume before the product was collected by filtration and dried in vacuo to provide the title compound as a white solid hydrochloride (4,3 g, 69%) m.p. 186°-189° C. 1H NMR (DMSO-d6)δ 1.31 (3H, d, --CH3), 3.51-3.60 (1H, m, --CH--), 4.05 (1H, dd, --CH2 a-), 4.12 (1H, dd, --CH2 b-), 6.95-7.00 (3H, m. Ar--H), 7.32 (2H, t, Ar--H).

후처리

  1. customwas formed
  2. concentrationThe reaction mixture was concentrated to half the original volume before the product
  3. filtrationwas collected by filtration
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-6a4de2790c414dfc9e37f1da5f881710
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05672588

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