反应 #4174246
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ed2b9db077ef4aa48718e9ae69406fa4暂无可渲染的结构数据
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呋喃-2-甲硫醇(CAS 175236-33-6)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ed2b9db077ef4aa48718e9ae69406fa4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d1480d654b4c4b789eca46cd0f6b9997反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-602125f09ae34eeaa89981b096b67e27反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d92077441d6e46d69d36e1da4f77a903反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9370f164905e4f5e89b7045f2e095b3d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b5cc3a88a7144a06971ef0965fbf3c59反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Example 52 is prepared from furfuryl mercaptan and 1d using the procedure described for compound 20.
来源 ID: ord-082305a78e0b4393b7faab34a3bc8589反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3.3 ml of a 30% sodium methylate solution in methanol is added in drops to 1.77 ml of furan-2-yl-methanethiol in 18 ml of anhydrous acetonitrile at 0° C. After 5 minutes, the drop-by-drop addition of 2.6 ml of 1-bromo-3-chloropropane is carried out. Then, the reaction solution is allowed to stir for 5 hours at room temperature. For working-up, the batch is diluted with ethyl acetate, washed with water and common salt solution, dried on magnesium sulfate and concentrated by evaporation in a vacuum. Chromatography of the crude product on silica gel with a hexane-ethyl acetate gradient yields 1.1 g of 2-(3-chloropropylthiomethyl)-furan as an oil. washed with water and common salt solution dried on magnesium sulfate concentrated by evaporation in a vacuum
来源 ID: ord-ade08c064c7145ec933f473d7fa31abc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (s)-3-tert-butoxycarbonylamino-1-chloro-2-heptanone (6.54 g) and furfurylmercaptan (3.11 g) in tetrahydrofuran (200 ml) was added 2N sodium hydroxide (13 ml), and the mixture was stirred at room temperature for 17 hours. Then, aqueous sodium hydrogencarbonate was added to the mixture, which was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate and filtered. The filtrate was concentrated and chromatographed on a silica gel column, eluting with hexane containing 10 % ethyl acetate to give the titled product (7.82 g). was extracted with ethyl acetate The extract was washed with saturated brine dried over magnesium sulfate filtered The filtrate was concentrated chromatographed on a silica gel column eluting with hexane containing 10 % ethyl acetate
来源 ID: ord-c9d60a9c699944a3a349fbb608f097b9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d1480d654b4c4b789eca46cd0f6b9997反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-602125f09ae34eeaa89981b096b67e27反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: a. Furfurylthiol acetate was prepared by reacting acetic chloride or anhydride with furfurylmercaptan according to the method described in Houben-Weyl, 4th ed., vol. 9, 753 (1955). The product has a b.p. of 90°-92°C./12 mm. Hg.
来源 ID: ord-07f1ec06cda448a284020684e1e63998PubChem References
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