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丙酮 → Methyl 3-Azidomethyl-2-thienyl Ketone

HRID 2420249
笔记
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反应方程式

HRID 2420249 反应方程式
Br[CH2:2][C:3]1[CH:7]=[CH:6][S:5][C:4]=1[C:8]([CH3:10])=[O:9].CC(C)=O.[N-:15]=[N+:16]=[N-:17].[Na+]>O>[N:15]([CH2:2][C:3]1[CH:7]=[CH:6][S:5][C:4]=1[C:8]([CH3:10])=[O:9])=[N+:16]=[N-:17]
参与物实验过程后处理来源与证据反应笔记

参与物

5

反应物 3

HCID 180丙酮HCID 33557叠氮化钠HCID 217012741-[3-(Bromomethyl)thiophen-2-yl]ethan-1-one

产物 1

HCID 20381562Methyl 3-Azidomethyl-2-thienyl Ketone

试剂、催化剂与溶剂 1

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]溶剂

实验过程

To a solution of methyl 3-bromomethyl-2-thienyl ketone (5 g., 0.023 mole) in 42 ml. of acetone and 4 ml. of water was added sodium azide (1.56 g., 0.024 mole) with caution (exothermic!). The resulting solution was stirred at room temperature for 2.5 hours, the acetone evaporated, the residue diluted with water and extracted with diethyl ether. The combined extracts were washed with water, saturated sodium bicarbonate solution and saturated sodium chloride solution, dried over magnesium sulfate and the dried extracts evaporated to dryness to obtain 4.0 g. (97%) of yellow oil. 1H--NMR (CDCl3), ppm. (δ): 7.5 (d, J=5, aromatic-H), 7.2 (d, J=5, aromatic-H), 4.75 (s, CH2N3), 2.5 (s, CH3); IR spectrum (film, cm.-1 : 3100, 2100 (N3), 1660, 1525 and 1420.

后处理

  1. customthe acetone evaporated
  2. additionthe residue diluted with water
  3. extractionextracted with diethyl ether
  4. washThe combined extracts were washed with water, saturated sodium bicarbonate solution and saturated sodium chloride solution
  5. dry with materialdried over magnesium sulfate
  6. customthe dried extracts evaporated to dryness
  7. customto obtain 4.0 g

来源与证据

ORD记录
ord-1b88bccd4c9847f48245b472a7e1d562
来源数据集
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
专利号
US04110342

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记