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Tetrahydrofuran → tert-Butyl 4-(bromomethylidene)piperidine-1-carboxylate

HRID 1666431
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HRID 1666431 반응식
[Br:1][C:2](Br)=[C:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1.C1COCC1.[Cl-].[NH4+]>CO.[Zn]>[Br:1][CH:2]=[C:3]1[CH2:8][CH2:7][N:6]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:5][CH2:4]1
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참가 물질

6

반응물 3

HCID 8028TetrahydrofuranHCID 25517Ammonium ChlorideHCID 53486134Tert-butyl 4-(dibromomethylene)piperidine-1-carboxylate

생성물 1

HCID 45489892tert-Butyl 4-(bromomethylidene)piperidine-1-carboxylate수율 66.4%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 887
Methanol
용매

실험 절차

tert-Butyl 4-(dibromomethylene)piperidine-1-carboxylate (64 g, 0.18 mol) was dissolved in methanol (438 mL) and THF (220 mL) and the solution was cooled to 0° C. Ammonium chloride (77.14 g, 1.44 mol) was added and the reaction was stirred for 30 min. Zinc dust (47.13 g, 0.72 mol) was added and the reaction mixture was stirred at RT for 2.5 h. The mixture was filtered and the filtrate was evaporated to dryness. The residue was purified by silica gel chromatography using 230-400 mesh silica gel (2% ethyl acetate in hexane) to give the title compound (33 g). 1H NMR (500 MHz, CDCl3): δ 5.99 (s, 1H), 3.40 (m, 4H), 2.38 (m, 2H), 2.23 (m, 2H), 1.47 (s, 9H).

후처리

  1. stirringthe reaction mixture was stirred at RT for 2.5 h
  2. filtrationThe mixture was filtered
  3. customthe filtrate was evaporated to dryness
  4. customThe residue was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-d640c2f015594ded925c34275600eb31
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044052B2

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