1,4-Dioxane-2,6-dione → HCID 86619729, 화합물

HRID 254689노트

반응식

HRID 254689 반응식
[N:1]([CH2:4][CH2:5][O:6][CH2:7][CH2:8][O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][NH2:21])=[N+:2]=[N-:3].[C:22]1(=[O:29])[O:28][C:26](=[O:27])[CH2:25][O:24][CH2:23]1>ClCCl.O>[N:1]([CH2:4][CH2:5][O:6][CH2:7][CH2:8][O:9][CH2:10][CH2:11][O:12][CH2:13][CH2:14][O:15][CH2:16][CH2:17][O:18][CH2:19][CH2:20][NH:21][C:26](=[O:27])[CH2:25][O:24][CH2:23][C:22]([OH:29])=[O:28])=[N+:2]=[N-:3]

참가 물질

5

반응물 2

HCID 782321,4-Dioxane-2,6-dioneHCID 2189447617-Azido-3,6,9,12,15-pentaoxaheptadecan-1-amine

생성물 1

HCID 86619729HCID 86619729, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매2회

실험 절차

To a solution of 17-azido-3,6,9,12,15-pentaoxaheptadecanamine (15 g, 50 mmol) in dichloromethane (100 mL) was added diglycolic anhydride (Acros, 6.4 g, 55 mmol). The reaction mixture was stirred overnight. The reaction was monitored by ESI-MS analysis, and more reagents were added to drive the reaction to completion. The solution was concentrated to give a yellow residue which was dissolved in water (250 mL). The product was isolated from the aqueous phase by continuous extraction with dichloromethane over night. Drying and evaporation of the solvent gave a yield of 18 g (85%). The product was characterized by ESI-MS analysis (MH+ calculated: 423.20; found 423.4). The product was used in the next step without further purification.

후처리

  1. additionwere added
  2. customthe reaction to completion
  3. concentrationThe solution was concentrated
  4. customto give a yellow residue which
  5. customDrying
  6. customevaporation of the solvent
  7. customgave a yield of 18 g (85%)
  8. customThe product was used in the next step without further purification

출처 및 근거

ORD 기록
ord-0f9774b2c208400080d77ef1dad759b3
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07875701B2

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