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Butyl isocyanate → HCID 4520152, 화합물

HRID 542490
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HRID 542490 반응식
[C:1]([O:10][CH3:11])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[CH2:12]([N:16]=[C:17]=[O:18])[CH2:13][CH2:14][CH3:15]>O1CCCC1>[CH2:12]([NH:16][C:17](=[O:18])[NH:4][C:3]1[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[C:1]([O:10][CH3:11])=[O:9])[CH2:13][CH2:14][CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8110Butyl isocyanateHCID 8635Methyl Anthranilate

생성물 1

HCID 4520152HCID 4520152, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 13.55 gm of methyl anthranilate in 12 ml dry tetrahydrofuran, was added 8.9 ml of n-butyl isocyanate dropwise. The solution was stirred for 51/2 days and filtered. The filtrate was reduced to half of its original volume and further precipitated with hexane and filtered. The two residues were combined to yield the title compound as a white solid, m.p. 84°-85° C.; NMR(delta CDCl3): 0.79, 1.02 (m, 3H, CH3), 1.16-1.76 (m, 4H, CH2CH2), 3.27 (t, 2H, NCH2), 3.87 (s, 3H, OCH3), 4.82 (br, 1H, NH), 6.81-8.59 (m, 4H, ArH), 11.09 (s, 1H, NH). IR: 3305, 3260, 1708, 1642, 1560 cm-1.

후처리

  1. filtrationfiltered
  2. customfurther precipitated with hexane
  3. filtrationfiltered

출처 및 근거

ORD 기록
ord-e926a7a7999842c08aef8994744e70fb
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04657893

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