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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Morpholine → 4-(3-Nitrobenzyl)morpholine

HRID 255036
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HRID 255036 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([N+:9]([O-:11])=[O:10])[CH:4]=1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.C(N(CC)CC)C>C1COCC1>[N+:9]([C:5]1[CH:4]=[C:3]([CH:8]=[CH:7][CH:6]=1)[CH2:2][N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1)([O-:11])=[O:10]
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참가 물질

5

반응물 3

HCID 8083MorpholineHCID 8471TriethylamineHCID 77568Benzene, 1-(bromomethyl)-3-nitro-

생성물 1

HCID 7832314-(3-Nitrobenzyl)morpholine수율 94%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 1-bromomethyl-3-nitrobenzene (2.16 g, 10 mmol), morpholine (1.76 g, 20.2 mmol) and triethylamine (1.0 mL) in THF (60 mL) was heated for two hours at 60° C. The solvent was evaporated, water was added and the product was isolated by extraction with ether. The ether extract was dried over Mg2SO4 and the solvent was evaporated. The crystalline residue was used in the next step without further purification. The product, 4-(3-nitrobenzyl)morpholine, was obtained in 94% yield (2.09 g).

후처리

  1. customThe solvent was evaporated
  2. additionwater was added
  3. customthe product was isolated by extraction with ether
  4. extractionThe ether extract
  5. dry with materialwas dried over Mg2SO4
  6. customthe solvent was evaporated
  7. customThe crystalline residue was used in the next step without further purification

출처 및 근거

ORD 기록
ord-b9fde5b032db4a4e86c6f0cfbdde9e71
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07875728B2

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