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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Iodide → HCID 131712367, 화합물

HRID 1982618
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HRID 1982618 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[Cl:12])[NH:5][CH2:6][CH2:7]Cl.[C:13]([NH2:17])([CH3:16])([CH3:15])[CH3:14].[I-].[Na+]>C(OCC)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([NH:5][CH2:6][CH2:7][NH:17][C:13]([CH3:16])([CH3:15])[CH3:14])[CH:9]=[CH:10][C:11]=1[Cl:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 6385Tert-ButylamineHCID 233170893,4-dichloro-N-(2-chloroethyl)aniline

생성물 1

HCID 131712367HCID 131712367, 화합물수율 159.4%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

15.0 g of 2-(3,4-dichloroanilino)ethylchloride, 19.2 g of tert.butylamine and approximately 1 g of sodium iodide were stirred for 26 hours at 90° C. After having been left to stand the weekend over at room temperature, the product was taken up in diethyl ether, washed with successively 2N sodium hydroxide solution and sodium bicarbonate solution and dried. After evaporating the solvent, 15.85 g of product were obtained, which were purified by column chromatography and then converted into the HCl salt with an alcoholic HCl solution. Melting point 206°-207° C.

후처리

  1. waitAfter having been left
  2. customover at room temperature
  3. washwashed with successively 2N sodium hydroxide solution and sodium bicarbonate solution
  4. customdried
  5. customAfter evaporating the solvent

출처 및 근거

ORD 기록
ord-007231858c934a06a6c47afb80327435
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04596891

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