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Hydrochloric Acid → 4-Bromo-2-(chloromethyl)-1-methylbenzene

HRID 716453
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HRID 716453 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:10])=[C:6]([CH:9]=1)[CH:7]=O.[BH4-].[Na+].CO.[ClH:15]>C1COCC1.O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:10])=[C:6]([CH:9]=1)[CH2:7][Cl:15]
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 4311764Sodium borohydrideHCID 104202895-Bromo-2-methylbenzaldehyde

생성물 1

HCID 128530964-Bromo-2-(chloromethyl)-1-methylbenzene

시약·촉매·용매 2

HCID 962Water용매
HCID 8028
Tetrahydrofuran
용매

반응 조건

온도
2.5 °C

실험 절차

To a mixture of 80.9 g (0.406 mol) of 5-bromo-2-methylbenzaldehyde and 7.80 g (0.206 mol) of NaBH4 in 300 ml of THF 200 ml of methanol was added dropwise by vigorous stirring for 5 h at 0-5° C. This mixture was stirred overnight at room temperature and then added to 1 liter of cold water. The resulting mixture was acidified by 2 M HCl to pH˜1, and the formed (5-bromo-2-methylphenyl)methanol was extracted with 3×250 ml of dichloromethane. The combined organic extract was dried over Na2SO4 and evaporated to dryness. To the residue dissolved in 450 ml of dichloromethane 37 ml of SOCl2 was added dropwise at +5° C. The resulting solution was stirred overnight at room temperature, evaporated to dryness, the residue was dissolved in 500 ml CH2Cl2, and the obtained solution was washed with 500 ml of water. The organic layer was separated, the aqueous layer was additionally extracted with 2×100 ml of dichloromethane. The combined organic extract was passed through a short pad of silica gel 60 (40-63 um), the filtrate was evaporated to dryness, and the residue was dried in vacuum to yield 5-bromo-2-methylbenzyl chloride as a slightly yellowish liquid which was further used without an additional purification.

후처리

  1. additionwas added dropwise
  2. stirringThis mixture was stirred overnight at room temperature
  3. extractionthe formed (5-bromo-2-methylphenyl)methanol was extracted with 3×250 ml of dichloromethane
  4. extractionThe combined organic extract
  5. dry with materialwas dried over Na2SO4
  6. customevaporated to dryness
  7. dissolutionTo the residue dissolved in 450 ml of dichloromethane 37 ml of SOCl2
  8. additionwas added dropwise at +5° C
  9. stirringThe resulting solution was stirred overnight at room temperature
  10. customevaporated to dryness
  11. dissolutionthe residue was dissolved in 500 ml CH2Cl2
  12. washthe obtained solution was washed with 500 ml of water
  13. customThe organic layer was separated
  14. extractionthe aqueous layer was additionally extracted with 2×100 ml of dichloromethane
  15. extractionThe combined organic extract
  16. customthe filtrate was evaporated to dryness
  17. customthe residue was dried in vacuum

출처 및 근거

ORD 기록
ord-86ccb2294a5a40ed9ab3a28144e4a281
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187583B2

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