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Hydrochloric Acid → Phenol, 4-(2-benzothiazolyl)-2,6-dimethoxy-

HRID 1243262
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HRID 1243262 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[S:14][C:15]3[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=3[N:17]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9]C.[Cl-].[Cl-].[Cl-].[Al+3].Cl>C(=S)=S>[OH:9][C:8]1[C:3]([O:2][CH3:1])=[CH:4][C:5]([C:13]2[S:14][C:15]3[CH:21]=[CH:20][CH:19]=[CH:18][C:16]=3[N:17]=2)=[CH:6][C:7]=1[O:11][CH3:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 6273072-(3,4,5-Trimethoxyphenyl)-1,3-benzothiazoleHCID 6451240Aluminum(III) Chloride

생성물 1

HCID 4156007Phenol, 4-(2-benzothiazolyl)-2,6-dimethoxy-수율 78.7%

시약·촉매·용매 1

HCID 6348Carbon Disulfide용매

실험 절차

A solution of 2-(3,4,5-trimethoxyphenyl)benzothiazole (4.0 g), aluminium trichloride (4.0 g) and carbon disulphide (75 cm3) was stirred at room temperature overnight. The reaction mixture was poured onto 20% hydrochloric acid (500 cm3) and extracted with ethyl acetate (3×50 cm3). The combined organic extracts were washed with water (2×250 cm3), dried (MgSO4), filtered and the filtrate evaporated down under reduced pressure. The solid residue was recrystallised from ethyl acetate to give 3.0 g (75.0%) of the desired product.

후처리

  1. extractionextracted with ethyl acetate (3×50 cm3)
  2. washThe combined organic extracts were washed with water (2×250 cm3)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customthe filtrate evaporated down under reduced pressure
  6. customThe solid residue was recrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-4f40a7bc320946d1822bce4c01ca62b2
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07118787B2

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