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Water → HCID 23458237, 화합물

HRID 1679949
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HRID 1679949 반응식
[I-].[CH3:2][C:3]([CH3:13])([CH3:12])[C:4](=[O:11])[CH2:5][CH2:6][N+](C)(C)C.[Cl:14][C:15]1[CH:16]=[CH:17][C:18]([NH:21][C:22](=[S:24])[S-:23])=[N:19][CH:20]=1.C([NH+](CC)CC)C.O>C(#N)C>[Cl:14][C:15]1[CH:16]=[CH:17][C:18]([NH:21][C:22](=[S:23])[S:24][CH2:6][CH2:5][C:4](=[O:11])[C:3]([CH3:2])([CH3:12])[CH3:13])=[N:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 43393N,N,N,4,4-Pentamethyl-3-oxopentan-1-aminium iodideHCID 23458243HCID 23458243, 화합물

생성물 1

HCID 23458237HCID 23458237, 화합물수율 60.1%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

(4,4-Dimethyl-3-oxopentyl)-trimethylammonium iodide (6.0 g) is added, at 20° C., to a suspension of triethylammonium 5-chloropyrid-2-yldithiocarbamate (6.1 g) in anhydrous acetonitrile (25 cc). The reaction is allowed to proceed for 6 hours at 20° C. Distilled water (25 cc) is added. The crystals which have appeared are filtered off, washed three times with distilled water (30 cc in total) and dried in air at 20° C. The resulting product (5.1 g; m.p.=110° C.) is recrystallised from acetonitrile (15 cc). 4,4-Dimethyl-3-oxopentyl 5-chloropyrid-2-yldithiocarbamate (3.8 g), which melts at 111° C., is obtained.

후처리

  1. filtrationThe crystals which have appeared are filtered off
  2. washwashed three times with distilled water (30 cc in total)
  3. customdried in air at 20° C
  4. customThe resulting product (5.1 g; m.p.=110° C.) is recrystallised from acetonitrile (15 cc)

출처 및 근거

ORD 기록
ord-3ee3fb1e9515444e99da6c5f21a3a779
출처 데이터셋
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04271167

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