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20,20'-(2-Hydroxy-1,3-propanediyl)bis(2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro(5.1.11.2)heneicosan-21-one) → HCID 19046706, 화합물

HRID 1781600
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HRID 1781600 반응식
[OH:1][CH:2]([CH2:30][N:31]1[C:44](=[O:45])[C:34]2([CH2:39][C:38]([CH3:41])([CH3:40])[NH:37][C:36]([CH3:43])([CH3:42])[CH2:35]2)[O:33][C:32]21[CH2:56][CH2:55][CH2:54][CH2:53][CH2:52][CH2:51][CH2:50][CH2:49][CH2:48][CH2:47][CH2:46]2)[CH2:3][N:4]1[C:17](=[O:18])[C:7]2([CH2:12][C:11]([CH3:14])([CH3:13])[NH:10][C:9]([CH3:16])([CH3:15])[CH2:8]2)[O:6][C:5]21[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2>C(OC(=O)C)(=O)C>[C:2]([O:1][CH:2]([CH2:3][N:4]1[C:17](=[O:18])[C:7]2([CH2:12][C:11]([CH3:14])([CH3:13])[N:10]([C:17](=[O:18])[CH3:7])[C:9]([CH3:16])([CH3:15])[CH2:8]2)[O:6][C:5]21[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)[CH2:30][N:31]1[C:44](=[O:45])[C:34]2([CH2:35][C:36]([CH3:42])([CH3:43])[N:37]([C:5](=[O:6])[CH3:19])[C:38]([CH3:40])([CH3:41])[CH2:39]2)[O:33][C:32]21[CH2:56][CH2:55][CH2:54][CH2:53][CH2:52][CH2:51][CH2:50][CH2:49][CH2:48][CH2:47][CH2:46]2)(=[O:1])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 1112563020,20'-(2-Hydroxy-1,3-propanediyl)bis(2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro(5.1.11.2)heneicosan-21-one)

생성물 1

HCID 19046706HCID 19046706, 화합물

시약·촉매·용매 1

HCID 7918Acetic Anhydride용매

실험 절차

39.2 g of 20,20'-(2-hydroxy-1,3-propanediyl)bis[2,2,4,4-tetramethyl-7-oxa-3,20-diazadispiro[5.1.11.2]heneicosan-21-one] were dissolved in 400 cm3 of acetic anhydride and heated so strongly that about 200 cm3 of liquid distilled off over the course of 6 hours. The batch was then evaporated to dryness in vacuo, the residue was taken up in toluene and washed by shaking with dilute hydrogencarbonate solution and water, and the organic phase was dried. After evaporation, the target compound crystallized as a colorless solid during stirring with hexane. 36.9 g having a melting point of 122° C. were obtained.

후처리

  1. distillationdistilled off over the course of 6 hours
  2. customThe batch was then evaporated to dryness in vacuo
  3. washwashed
  4. customthe organic phase was dried
  5. customAfter evaporation
  6. customthe target compound crystallized as a colorless solid
  7. stirringduring stirring with hexane
  8. customwere obtained

출처 및 근거

ORD 기록
ord-386686c9206a4c6aa84bffbf027ce9a8
출처 데이터셋
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05633378

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