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Tin tetrachloride → HCID 18430715, 화합물

HRID 1954287
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HRID 1954287 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([CH2:13][CH3:14])[C:10]=1[O:11][CH3:12])[C:5]([OH:7])=O.[C:15](Cl)(=[O:19])[C:16](Cl)=O.[Sn](Cl)(Cl)(Cl)Cl.[CH2:26]([C:33]1(C)[CH:37](C)[CH:36]=[CH:35]O1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH2:26]([C:33]1[O:19][C:15]([CH3:16])=[C:36]([CH3:35])[C:37]=1[C:5]([C:4]1[CH:8]=[C:9]([CH2:13][CH3:14])[C:10]([O:11][CH3:12])=[C:2]([Br:1])[CH:3]=1)=[O:7])[C:27]1[CH:28]=[CH:29][CH:30]=[CH:31][CH:32]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 24287Tin tetrachlorideHCID 65578Oxalyl chlorideHCID 18430741HCID 18430741, 화합물HCID 23296013HCID 23296013, 화합물

생성물 1

HCID 18430715HCID 18430715, 화합물수율 96.2%

실험 절차

The title compound was prepared according to the procedure in Example 1, step 4, using 3-bromo-5-ethyl-4-methoxybenzoic acid (4.95 g, 19.1 mmol), oxalyl chloride (1.8 mL, 20.7 mmol), N,N-DMF (2 drops), tin(IV) chloride (2.50 mL, 21.4 mmol) and 2-benzyl-2,3-dimethylfuran (4.30 g, 23.1 mmol) to give 7.85 g (96%) of the title compound. 1H NMR: consistent.

후처리

  1. customThe title compound was prepared

출처 및 근거

ORD 기록
ord-3d8ba9eed8ee4a2a98a018b9cb51cbf9
출처 데이터셋
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06121271

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