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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 4549261, 화합물

HRID 1393682
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HRID 1393682 반응식
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][CH:3]=1.[S-:11][C:12]#[N:13].[NH4+].BrBr.O>CO>[NH2:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[S:11][C:12]#[N:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 9784-Aminobenzoic AcidHCID 15666Ammonium thiocyanateHCID 24408Bromine

생성물 1

HCID 4549261HCID 4549261, 화합물수율 53.4%

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
-15 °C

실험 절차

4-Aminobenzoic acid (13 g) and ammonium thiocyanate (6.9 g) were suspended in methanol (200 ml) and cooled at −15° C. on an ice bath. A methanol solution (40 ml) containing bromine (4.7 ml) was added slowly dropwise thereto. The mixture was warmed to room temperature and stirred for 2 hours, iced water (500 ml) was added thereto, and precipitated crystals were collected by filtration and washed with water and n-hexane. The product was dried under reduced pressure to give 4-amino-3-thiocyanatobenzoic acid (9.4 g, Y.:53%) as white crystals.

후처리

  1. additionwas added slowly dropwise
  2. temperatureThe mixture was warmed to room temperature
  3. customprecipitated crystals
  4. filtrationwere collected by filtration
  5. washwashed with water and n-hexane
  6. customThe product was dried under reduced pressure

출처 및 근거

ORD 기록
ord-6b416339a8c54dfc93033a5c96c95d1f
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07345180B2

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