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Hydrochloric Acid → Benzenediazonium, 4-chloro-, chloride

HRID 247352
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HRID 247352 반응식
C([O-])(=O)C.[Na+].CC1OC(=O)C=C(O)C=1C(OC)=O.N([O-])=O.[Na+].[Cl:23][C:24]1[CH:30]=[CH:29][C:27]([NH2:28])=[CH:26][CH:25]=1.Cl.O1C=CC=CC1=O.[NH:39]1CCOCC1>O.CO>[Cl-:23].[Cl:23][C:24]1[CH:30]=[CH:29][C:27]([N+:28]#[N:39])=[CH:26][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 7

HCID 313Hydrochloric AcidHCID 78124-ChloroanilineHCID 8083MorpholineHCID 681542H-Pyran-2-oneHCID 517045Sodium AcetateHCID 23668193Sodium NitriteHCID 547195216-Methyl-5-carbomethoxy-4-hydroxy-2-pyrone

생성물 1

HCID 11819533
Benzenediazonium, 4-chloro-, chloride

시약·촉매·용매 2

HCID 887Methanol용매2회HCID 962Water용매2회

실험 절차

A 250 ml, three necked, round bottomed flask was equipped with addition funnel, paddle stirrer, and thermometer. The flask was charged with 50 ml methanol, sodium acetate (16.0 g, 0.198 mole), and 6-methyl-5-carbomethoxy-4-hydroxy-2-pyrone (8.0 g, 0.43 mole). p-Chlorobenzenediazonium chloride was prepared on the side by the dropwise addition of sodium nitrite (3.3 g, 0.047 mole) in 10 ml water to a cooled (5°) slurry containing p-chloroaniline (5.6 g, 0.043 mole) in aqueous hydrochloric acid (16.5 ml 12N HCl [0.198 mole] plus 10 ml water). The diazonium chloride solution was added dropwise to the solution containing the pyrone. This addition was carried out during 10 min. with no noticeable exotherm. After complete addition, the resulting orange slurry was stirred for 40 min. at room temperature. Suction filtration gave an orange filter cake which was washed repeatedly with water, then sucked dry during 2 hr. The filter cake thus obtained was placed back into the three necked flask used above. Methanol (200 ml) was added to give a slurry. Morpholine (10.0 g., 0.115 mole) was added in one portion. A mildly exothermic reaction occurred, and a dark, homogeneous solution was obtained. After stirring 10 min., the solution was poured into 300 ml water. This was extracted with methylene chloride (3×100 ml). The combined organic extracts were extracted repeatedly with dilute aqueous sodium hydroxide (pH 8). The combined aqueous basic layers were acidified with 6N hydrochloric acid. With cooling and scratching, a solid crystallized from solution. Suction filtration gave (V) as a light brown powder (8.2 g, 60% yield based on pyrone). NMR (CDCl3): 7.5 ppm (multiplet, 4H); 4.0 (S, 3H); 2.3 (S, 3H). IR (CH2Cl2): 5.75, 6.22, 6.90, mp 203-204 (dec.). An analytical sample was crystallized from methanol.

후처리

  1. customA 250 ml, three necked, round bottomed flask was equipped with addition funnel, paddle stirrer
  2. temperaturea cooled (5°) slurry
  3. additionThis addition
  4. additionAfter complete addition
  5. filtrationSuction filtration
  6. customgave an orange filter cake which
  7. washwas washed repeatedly with water
  8. customsucked dry during 2 hr
  9. customThe filter cake thus obtained
  10. customto give a slurry
  11. customA mildly exothermic reaction
  12. customa dark, homogeneous solution was obtained
  13. stirringAfter stirring 10 min.
  14. extractionThis was extracted with methylene chloride (3×100 ml)
  15. extractionThe combined organic extracts were extracted repeatedly with dilute aqueous sodium hydroxide (pH 8)
  16. temperatureWith cooling
  17. customa solid crystallized from solution
  18. filtrationSuction filtration

출처 및 근거

ORD 기록
ord-d1490f1d3e60438ca5c1e07a2742c283
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04707181

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