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Thionyl Chloride → N-(4-(1-chloroethyl)phenylmethyl)acetamide

HRID 1282104
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HRID 1282104 반응식
O[CH:2]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][NH:11][C:12](=[O:14])[CH3:13])=[CH:6][CH:5]=1)[CH3:3].S(Cl)([Cl:17])=O.C(=O)([O-])O.[Na+]>C(Cl)(Cl)Cl>[Cl:17][CH:2]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][NH:11][C:12](=[O:14])[CH3:13])=[CH:6][CH:5]=1)[CH3:3]
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참가 물질

5

반응물 3

HCID 24386Thionyl ChlorideHCID 516892Sodium BicarbonateHCID 18423003HCID 18423003, 화합물

생성물 1

HCID 18423036N-(4-(1-chloroethyl)phenylmethyl)acetamide

시약·촉매·용매 1

HCID 6212Chloroform용매2회

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온도
30 °C

실험 절차

To a solution of N-(4-(1-hydroxyethyl)phenylmethyl)acetamide (5.26 g) in chloroform (40 ml) was added dropwise a solution of thionyl chloride (2.1 ml) in chloroform (10 ml) at below 5° C. over 20 min. The mixture was stirred at 30° C. for 1 hr. The mixture was poured into a saturated sodium hydrogencarbonate solution and extracted with chloroform. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (elution solvent; methanol:chloroform=4:96) to give the title compound (4.08 g) as white crystals.

후처리

  1. extractionextracted with chloroform
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. customthe solvent was evaporated
  4. customThe obtained residue was purified by silica gel column chromatography (elution solvent; methanol:chloroform=4:96)

출처 및 근거

ORD 기록
ord-942abe6408a74c4082bf59132c2ae5c8
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06455528B1

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