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Hydrochloric Acid → HCID 54377319, 화합물

HRID 2227111
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HRID 2227111 반응식
[CH3:1][C:2]1[CH2:7][CH2:6][CH:5]([OH:8])[CH2:4][CH:3]=1.[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1.Cl>N1C=CC=CC=1>[S:15]([O:8][CH:5]1[CH2:6][CH2:7][C:2]([CH3:1])=[CH:3][CH2:4]1)([C:12]1[CH:13]=[CH:14][C:9]([CH3:19])=[CH:10][CH:11]=1)(=[O:17])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 73974-Toluenesulfonyl chlorideHCID 12882493HCID 12882493, 화합물

생성물 1

HCID 54377319HCID 54377319, 화합물

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of alcohol 4C (R=methyl) (10 g) and p-toluenesulfonyl chloride (20.8 g) in anhydrous tetrahydrofaran (21 mL) at 0° C. is added anhydrous pyridine (21 mL). The reaction is allowed to stir in an ice bath for 2 hours, and is then allowed to stand at −20° C. for a further 16 hours. The reaction mixture is then poured into 2M HCl (75 mL) and extracted with ethyl acetate. The combined organic layers are extracted with brine and dried over sodium sulfate. The solvent is removed in vacuo.

후처리

  1. waitto stand at −20° C. for a further 16 hours
  2. extractionextracted with ethyl acetate
  3. extractionThe combined organic layers are extracted with brine
  4. dry with materialdried over sodium sulfate
  5. customThe solvent is removed in vacuo

출처 및 근거

ORD 기록
ord-af340bcbabd44571b598eba2f270674c
출처 데이터셋
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06413448B1

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