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Benzaldehyde → HCID 67441412, 화합물

HRID 389938
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HRID 389938 반응식
COP([CH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([Br:16])[CH:14]=2)[C:9](=[O:17])[O:8]1)(=O)OC.[CH:18](=O)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(N(CC)CC)C.O>O1CCCC1>[CH:18](=[C:7]1[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([Br:16])[CH:14]=2)[C:9](=[O:17])[O:8]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 240BenzaldehydeHCID 962WaterHCID 8471TriethylamineHCID 87401836HCID 87401836, 화합물

생성물 1

HCID 67441412HCID 67441412, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of EXAMPLE 1C (4.6 g, 14.08 mmol) in anhydrous tetrahydrofuran (30 mL) was added benzaldehyde (0.71 mL, 7.4 mmol) and triethylamine (1.00 mL, 7.39 mmol). The reaction mixture was stirred at ambient temperature overnight. Water was added and the mixture stirred for 10 minutes. The precipitated solid was filtered and dried under vacuum to yield the title compound. MS (ESI) m/z 302 (M+H)+.

후처리

  1. stirringthe mixture stirred for 10 minutes
  2. filtrationThe precipitated solid was filtered
  3. customdried under vacuum

출처 및 근거

ORD 기록
ord-9170f68ee52947488e12513a3e2796d9
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08383623B2

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