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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Aniline → Chloroacetanilide

HRID 38707
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HRID 38707 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[Cl:15][CH2:16][C:17](Cl)=[O:18]>C1COCC1>[Cl:15][CH2:16][C:17]([NH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6115AnilineHCID 6577Chloroacetyl chlorideHCID 8471Triethylamine

생성물 1

HCID 11485Chloroacetanilide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of aniline (9.31 g, 100 mmol) and triethylamine (15.2 g, 150 mmol) in THF (150 mL) is cooled to −40° C. before chloroacetic acid chloride (11.3 g, 100 mmol) is slowly added in portions such that the temperature does not rise above 0° C. After completion of the addition, the brown suspension is stirred at rt for 1 h. The dark purple mixture is poured onto water (300 mL) and extracted twice with EA (300 mL). The organic extracts are washed with sat. aq. NaHCO3, 0.5 N aq. HCl, followed by water, and evaporated. The brown residue is suspended in diethyl ether, filtered off, washed with additional diethyl ether and dried under high vacuum to give 2-chloro-N-phenyl-acetamide. LC-MS: tR=0.75 min, [M+1]+=170, 1H NMR (CDCl3): δ 8.22 (s br, 1H), 7.56-7.51 (m, 2H), 7.40-7.24 (m, 2H), 7.20-7.14 (m, 1H), 4.20 (s, 2H).

후처리

  1. additionis slowly added in portions such that the temperature
  2. customdoes not rise above 0° C
  3. additionAfter completion of the addition
  4. additionThe dark purple mixture is poured onto water (300 mL)
  5. extractionextracted twice with EA (300 mL)
  6. washThe organic extracts are washed with sat. aq. NaHCO3, 0.5 N aq. HCl
  7. customevaporated
  8. filtrationfiltered off
  9. washwashed with additional diethyl ether
  10. customdried under high vacuum

출처 및 근거

ORD 기록
ord-56994b97fd3d4d8780cb7480791f0e2f
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524752B2

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