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

HRID 1577048
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HRID 1577048 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 2 N 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 2 N sodium hydroxide solution and sodium bicarbonate solution
  4. customdried
  5. customAfter evaporating the solvent

출처 및 근거

ORD 기록
ord-9b740909c65a442f86d34d5b656a088a
출처 데이터셋
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04286983

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