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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Bromopropane → HCID 178460859, 화합물

HRID 260724
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HRID 260724 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][NH:9][C:10]([NH2:12])=[S:11].[CH2:13](Br)[CH2:14][CH3:15]>C(#N)C>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][NH:9][C:10](=[NH:12])[S:11][CH2:13][CH2:14][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 78401-BromopropaneHCID 22400378HCID 22400378, 화합물

생성물 1

HCID 178460859HCID 178460859, 화합물수율 78%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 1-(2-chlorophenyl)methyl thiourea (3 g, 14.9 mmol) and propylbromide (13.5 g, 110 mmol) in acetonitrile (20 mL) was refluxed for 5 hours. The solvent was evaporated, the residue was dissolved in 200 mL of 50% water/ether and acidified with 48% hydrobromic acid solution. The two phases were separated, the aqueous layer was washed with ether and then the aqueous layer was basified with 10% sodium carbonate solution. The liberated product was extracted with diethyl ether, washed with water and brine, dried and concentrated to give 1-(2-chlorophenyl)methyl-2-propyl-2-thiopseudourea (2.82 g, 78%); mp 112°-114° C.

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후처리

  1. temperaturewas refluxed for 5 hours
  2. customThe solvent was evaporated
  3. dissolutionthe residue was dissolved in 200 mL of 50% water/ether
  4. customThe two phases were separated
  5. washthe aqueous layer was washed with ether
  6. extractionThe liberated product was extracted with diethyl ether
  7. washwashed with water and brine
  8. customdried
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-629220f6940f4c29a1fb10c7dd7dc1b0
출처 데이터셋
uspto-grants-1996_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05530017

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