Hydrochloric Acid → 3-Bromo-5-chlorotoluene

HRID 1432054노트

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HRID 1432054 반응식
N[C:2]1[C:7]([Cl:8])=[CH:6][C:5]([Br:9])=[CH:4][C:3]=1[CH3:10].Cl.N([O-])=O.[Na+].O[PH2]=O>C(O)(=O)C.O>[Cl:8][C:7]1[CH:2]=[C:3]([CH3:10])[CH:4]=[C:5]([Br:9])[CH:6]=1

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 27696264-Bromo-2-chloro-6-methylanilineHCID 4124402Phosphinic AcidHCID 23668193Sodium Nitrite

생성물 1

HCID 107746383-Bromo-5-chlorotoluene수율 81.1%

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매2회

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온도
0 °C

실험 절차

Step G1. To an ice-water-cooled and stirred solution of 2-amino-5-bromo-3-chlorotoluene (12 g, 54 mmol) in a mixture of 100 mL of acetic acid, 43 mL of H2O and 11.5 mL of concentrated HCl was added dropwise a solution of NaNO2 (4.48 g, 65 mmol) in 15 mL of H2O. The reaction mixture was stirred for 30 min and was then added to an 112 mL solution of 50% H3PO2 cooled at 0° C. After being stirred for 6 h at 0° C., the reaction mixture was allowed to stand at room temperature overnight. The solid was filtered and washed with water, then dried in vacuum. 3-Chloro-5-bromo-toluene (9 g, 81%) was obtained as brown solid. Crystals. 1H NMR (CDCl3): δ 2.31 (s, 3H), 7.10 (s, 1H), 7.21 (s, 1H), 7.31 (s, 1H).

후처리

  1. stirringAfter being stirred for 6 h at 0° C.
  2. waitto stand at room temperature overnight
  3. filtrationThe solid was filtered
  4. washwashed with water
  5. customdried in vacuum

출처 및 근거

ORD 기록
ord-7cd4a869a0af46ed929d026de4ddbe0f
출처 데이터셋
uspto-grants-2009_11
특허 번호
US07612069B2

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