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Formaldehyde → 3,5-Dichlorosalicyl alcohol

HRID 1462964
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HRID 1462964 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[OH:9].[OH-:10].[Na+].[CH2:12]=O>S(=O)(=O)(O)O>[Cl:1][C:2]1[C:3]([OH:9])=[C:4]([CH:5]=[C:6]([Cl:8])[CH:7]=1)[CH2:12][OH:10]
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참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 84492,4-DichlorophenolHCID 14798Sodium Hydroxide

생성물 1

HCID 2411963,5-Dichlorosalicyl alcohol

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

A mixture of 2,4-dichlorophenol (15.3 g), 10% sodium hydroxide solution (100 ml) and 40% aqueous formaldehyde solution (37.5 ml) was heated at 95°-100° C. for 4 hr, then cooled and acidified by addition of 2-normal sulphuric acid (70 ml). The precipitated oil was extracted into toluene, and the extract washed with sodium bicarbonate solution, dried and evaporated. The residue was recrystallised from boiling water to yield 3,5-dichloro-2-hydroxybenzyl alcohol (4.0 g), m.p. 81°-82° C. on drying at 56° C./20 mm. Hg=2660 Pa.

후처리

  1. temperaturewas heated at 95°-100° C. for 4 hr
  2. temperaturecooled
  3. extractionThe precipitated oil was extracted into toluene
  4. washthe extract washed with sodium bicarbonate solution
  5. customdried
  6. customevaporated
  7. customThe residue was recrystallised

출처 및 근거

ORD 기록
ord-3ada45b6e1414c3daf08adc4c2c5dc3f
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461907

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