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Hydrochloric Acid → (3-Chloro-3-methyl-2-nitrosobutoxy)benzene

HRID 1580586
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인쇄 미리보기

반응식

HRID 1580586 반응식
[ClH:1].[O:2]([CH2:9][CH:10]=[C:11]([CH3:13])[CH3:12])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[N:14]([O:16]CCCCC)=O>C(O)(=O)C>[Cl:1][C:11]([CH3:13])([CH:10]([N:14]=[O:16])[CH2:9][O:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1)[CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 10026Pentyl nitriteHCID 564931Benzene, ((3-methyl-2-butenyl)oxy)-

생성물 1

HCID 21316467(3-Chloro-3-methyl-2-nitrosobutoxy)benzene수율 50%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Concentrated hydrochloric acid (7.8 ml) was added dropwise over 1 hour to a mixture of 1-(p-methoxy)phenoxy-3-methylbut-2-ene (VI; R = CH2OC6H4.OCH3, R1 = R2 = CH3) (12.0 g) and amyl nitrite (11.7 ml) in glacial acetic acid (15.6 ml) at 0°C (ice-salt bath). A white precipitate separated and this was filtered off and dried to give the nitrosochloride (V) (8.0 g, yield 50%) as colourless crystals, m.p. 137°.

후처리

  1. customA white precipitate separated
  2. filtrationthis was filtered off
  3. customdried

출처 및 근거

ORD 기록
ord-09596566a1624646b2e2b936aafcff2c
출처 데이터셋
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03933820

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