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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrogen Sulfide → HCID 19848484, 화합물

HRID 1608123
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HRID 1608123 반응식
N1CCCCC1.[OH-].C([N+](C)(C)C)C1C=CC=CC=1.[CH:19]([N:21]([CH2:25][CH:26]=[CH2:27])[CH2:22][CH:23]=[CH2:24])=[O:20].[SH2:28]>CO>[CH:19]([N:21]1[CH2:25][CH:26]([CH3:27])[S:28][CH:23]([CH3:24])[CH2:22]1)=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 402Hydrogen Sulfide2회HCID 8082PiperidineHCID 66854Benzyltrimethylammonium hydroxideHCID 246338N,N-Diallylformamide

생성물 1

HCID 19848484HCID 19848484, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

Piperidine (10 ml) and 10 ml of a 40% solution of benzyltrimethylammoniumhydroxide in methanol were added to a solution of N-formyl-diallylamine (55 g) in methanol (200 ml). Hydrogen sulfide (50 g) was introduced into the resulting solution, and unreacted hydrogen sulfide was kept at reflux for 7 hours by means of "cold finger". The mixture was left at room temperature for 48 hours, flushed with nitrogen, diluted with ether, and washed with water. The organic phase was dried, and the solvent evaporated in vacuo. Distillation of the residue gave the title compound with boiling point 145° C./15 mmHg.

후처리

  1. temperatureat reflux for 7 hours by means of "cold finger"
  2. customflushed with nitrogen
  3. additiondiluted with ether
  4. washwashed with water
  5. customThe organic phase was dried
  6. customthe solvent evaporated in vacuo
  7. distillationDistillation of the residue

출처 및 근거

ORD 기록
ord-e0c489c0daac4c04bbda3865cc1b37aa
출처 데이터셋
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04870063

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