Carbon Tetrachloride → 2-Chloro-4-(oxan-4-yl)phenol

HRID 1678972노트

반응식

HRID 1678972 반응식
S(Cl)(Cl)(=O)=O.[OH:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)=[CH:9][CH:8]=1.C(Cl)(Cl)(Cl)[Cl:20]>[OH-].[Na+]>[OH:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]2[CH2:14][CH2:15][O:16][CH2:17][CH2:18]2)=[CH:9][C:8]=1[Cl:20]

참가 물질

5

반응물 3

HCID 5943Carbon TetrachlorideHCID 24648Sulfuryl chlorideHCID 227373584-(Oxan-4-yl)phenol

생성물 1

HCID 184146372-Chloro-4-(oxan-4-yl)phenol

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

10 ml of sulfuryl chloride were added with stirring to a mixture of 14.1 g of 4-(p-hydroxyphenyl)-tetrahydropyran and 40 ml of carbon tetrachloride and the mixture was heated to 45°-50° C for 16 hours. The mixture was concentrated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with methylene chloride yielded a crystal product which was dissolved in 200 ml of N sodium hydroxide and the solution was washed with ether and acidified with 2N hydrochloric acid. The mixture was extracted with ether and the organic phase was washed with water, then an aqueous sodium bisulfite solution and then with water. The extracts were dried and evaporated to dryness to obtain 6.4 g of 4-(4-hydroxy-3-chlorophenyl)-tetrahydropyran melting at 123°-125° C.

후처리

  1. temperaturethe mixture was heated to 45°-50° C for 16 hours
  2. concentrationThe mixture was concentrated to dryness under reduced pressure
  3. customthe residue was chromatographed over silica gel
  4. washElution with methylene chloride
  5. customyielded a crystal product which
  6. washthe solution was washed with ether
  7. extractionThe mixture was extracted with ether
  8. washthe organic phase was washed with water
  9. customThe extracts were dried
  10. customevaporated to dryness

출처 및 근거

ORD 기록
ord-3b17c930ff88481e8fd7784b76902d4a
출처 데이터셋
uspto-grants-1978_03
특허 번호
US04078076

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