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Citric Acid → 2-(4-(Heptyloxy)phenyl)-2-oxoethyl 4-bromobenzoate

HRID 1775838
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HRID 1775838 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[CH:7][CH:6]=1)=[O:4].[Br:19][C:20]1[CH:28]=[CH:27][C:23]([C:24]([OH:26])=[O:25])=[CH:22][CH:21]=1.C(O)(=O)CC(CC(O)=O)(C(O)=O)O.CC(=O)OCC>C(#N)C>[Br:19][C:20]1[CH:28]=[CH:27][C:23]([C:24]([O:26][CH2:2][C:3]([C:5]2[CH:10]=[CH:9][C:8]([O:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[CH:7][CH:6]=2)=[O:4])=[O:25])=[CH:22][CH:21]=1
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참가 물질

6

반응물 4

HCID 311Citric AcidHCID 8857Ethyl AcetateHCID 114644-Bromobenzoic acidHCID 539091862-Bromo-1-(4-(heptyloxy)phenyl)ethanone

생성물 1

HCID 866896872-(4-(Heptyloxy)phenyl)-2-oxoethyl 4-bromobenzoate수율 57%

시약·촉매·용매 1

HCID 6342Acetonitrile
용매

실험 절차

To a solution of 2-bromo-1-(4-(heptyloxy)phenyl)ethanone INT-4 (1.3 g, 4.2 mmol) and 4-bromobenzoic acid (0.70 g, 3.5 mmol) in ACN (30 mL) was added TEA (0.72 ml, 5.2 mmol). After stirring overnight, the mixture was poured onto aq. citric acid and EA then stirred for 10 min before the solid was collected by filtration. The cake was washed with water and iso-hexanes then dried to provide 905 mg (57%) of 2-(4-(heptyloxy)phenyl)-2-oxoethyl 4-bromobenzoate. LCMS-ESI (m/z) calculated for C22H25BrO4, 432.1. found 433.2 [M+H]+, tR=3.24 min (Method 8).

후처리

  1. stirringthen stirred for 10 min before the solid
  2. filtrationwas collected by filtration
  3. washThe cake was washed with water and iso-hexanes
  4. customthen dried

출처 및 근거

ORD 기록
ord-a601912b59d64b67835ac6ffd6b03ebc
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09260427B2

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