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Triphosgene → 4-Methoxycarbonylphenyl-pentyl-carbamoyl chloride

HRID 1759780
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HRID 1759780 반응식
[CH2:1]([NH:6][C:7]1[CH:16]=[CH:15][C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:9][CH:8]=1)[CH2:2][CH2:3][CH2:4][CH3:5].[Cl:17][C:18](Cl)([O:20]C(=O)OC(Cl)(Cl)Cl)Cl>C1COCC1>[CH3:14][O:13][C:11]([C:10]1[CH:9]=[CH:8][C:7]([N:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[C:18]([Cl:17])=[O:20])=[CH:16][CH:15]=1)=[O:12]
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참가 물질

4

반응물 2

HCID 94429TriphosgeneHCID 22600039Methyl 4-pentylaminobenzoate

생성물 1

HCID 226000294-Methoxycarbonylphenyl-pentyl-carbamoyl chloride수율 275.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of methyl 4-pentylaminobenzoate (43) (200 mg, 0.91 mmole) in 5 mL of THF was treated with 95 mg of triphosgene (0.35 eq.), stirred at reflux for three hours, then poured onto 50 mL ice-water and extracted with three portions of 50 mL of ethyl acetate. The combined organic extracts were dried over MgSO4, filtered and concentrated in vacuo to give 250 mg of 4-methoxycarbonylphenyl-pentyl-carbamoyl chloride (45) which was used without purification.

후처리

  1. temperatureat reflux for three hours
  2. extractionextracted with three portions of 50 mL of ethyl acetate
  3. dry with materialThe combined organic extracts were dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0e05fe2475d4436c8b0fc6578183d1b8
출처 데이터셋
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06838472B2

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