反応 #4174246
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ed2b9db077ef4aa48718e9ae69406fa4表示可能な構造データがありません
C1=COC(=C1)CS製品情報
Furfuryl mercaptan (CAS 98-02-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 7363
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ed2b9db077ef4aa48718e9ae69406fa4反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d1480d654b4c4b789eca46cd0f6b9997反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-602125f09ae34eeaa89981b096b67e27反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d92077441d6e46d69d36e1da4f77a903反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9370f164905e4f5e89b7045f2e095b3d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b5cc3a88a7144a06971ef0965fbf3c59反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Example 52 is prepared from furfuryl mercaptan and 1d using the procedure described for compound 20.
ソース ID: ord-082305a78e0b4393b7faab34a3bc8589反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-ade08c064c7145ec933f473d7fa31abc反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-c9d60a9c699944a3a349fbb608f097b9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-d1480d654b4c4b789eca46cd0f6b9997反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-602125f09ae34eeaa89981b096b67e27反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-07f1ec06cda448a284020684e1e63998PubChem References
化合物の公開データベース記録に掲載された情報源です。
