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Hydrochloric Acid → 3-Isopropylphenyl (chlorosulfinyl)(methyl)carbamate

HRID 67038
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HRID 67038 반응식
[CH3:1][NH:2][C:3](=[O:14])[O:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH:11]([CH3:13])[CH3:12])[CH:6]=1.[S:15](Cl)([Cl:17])=[O:16].Cl>>[Cl:17][S:15]([N:2]([CH3:1])[C:3](=[O:14])[O:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([CH:11]([CH3:12])[CH3:13])[CH:6]=1)=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 6143M-Cumenyl MethylcarbamateHCID 24386Thionyl Chloride

생성물 1

HCID 127288083-Isopropylphenyl (chlorosulfinyl)(methyl)carbamate

실험 절차

Four grams 3-isopropylphenyl methylcarbamate were mixed with excess thionyl chloride and heated up to 80° C. until HCl evolution ceased. Excess thionyl chloride was removed by distillation and the residue was subjected to high vacuum (0.1 mm) for 1 hour. NMR of the residue in chloroform-d-TMS gave the following absorptions: δ7.5-6.9 (m, 4H, aromatic protons). δ3.25 (s, 3H, NCH3), δ3.2-2.7 (m, 1H, CH), and δ1.3-1.2 (d, 6H, C(CH3 (2).

후처리

  1. customExcess thionyl chloride was removed by distillation
  2. customNMR of the residue in chloroform-d-TMS gave the following absorptions

출처 및 근거

ORD 기록
ord-43c8348170c04253ad35d8384e0a9578
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04344883

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