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

HRID 224375
ノート
印刷プレビュー

反応式

HRID 224375 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 31275
1,4-Dioxane
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-344b732e97e94e248037819139cdc6ee
出典データセット
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04232035

反応ノート

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