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Diisopropyl Ether → 4-[[O-[N-Methyl-N-(methylthiosulfenyl)carbamoyl]oximino]]-5-methyl-1,3-oxathiolane

HRID 224375
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반응식

HRID 224375 반응식
[CH3:1][CH:2]1[O:6][CH2:5][S:4][C:3]1=[N:7][OH:8].[CH3:9][N:10]([S:14][S:15][CH3:16])[C:11](F)=[O:12].C(N(CC)CC)C.C(OC(C)C)(C)C>O1CCOCC1>[CH3:9][N:10]([S:14][S:15][CH3:16])[C:11]([O:8][N:7]=[C:3]1[CH:2]([CH3:1])[O:6][CH2:5][S:4]1)=[O:12]
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참가 물질

6

반응물 4

HCID 7914Diisopropyl EtherHCID 8471TriethylamineHCID 20479042N-methyl-N-(methylthiosulfenyl) carbamoyl fluorideHCID 71364792N-(5-Methyl-1,3-oxathiolan-4-ylidene)hydroxylamine

생성물 1

HCID 539513834-[[O-[N-Methyl-N-(methylthiosulfenyl)carbamoyl]oximino]]-5-methyl-1,3-oxathiolane수율 1.9%

시약·촉매·용매 1

HCID 31275
1,4-Dioxane
용매

실험 절차

To a solution of 4.22 g (0.032 m) of 5-methyl-4-oximino-1,3-oxathiolane and 5.0 g (0.032 m) of N-methyl-N-(methylthiosulfenyl) carbamoyl fluoride in 25 ml of dioxane was added 3.25 g (0.032 m) of triethylamine. After stirring at room temperature for 19 hrs. the reaction mixture was quenched with 100 ml of water and extracted in ethyl acetate. After the usual work-up it yielded a residual oil. Addition of isopropyl ether resulted in the precipitation of 0.16 g of a solid biscarbamate. The concentrated filtrate was purified by column chromatography to yield 2.97 g of an oil.

후처리

  1. customthe reaction mixture was quenched with 100 ml of water
  2. extractionextracted in ethyl acetate
  3. customAfter the usual work-up it yielded a residual oil

출처 및 근거

ORD 기록
ord-344b732e97e94e248037819139cdc6ee
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04232035

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