反応 #4091171
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-787b95fd05694948bb9e0eecd8a1d368表示可能な構造データがありません
CCCCCCCCCCN=C=S製品情報
1-isothiocyanatodecane (CAS 24540-94-1) 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 90535
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
10 反応 · 10 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-787b95fd05694948bb9e0eecd8a1d368反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of compound AA (9.1 g) in dry N,N′-dimethylformamide (15 ml) was added n-decylisothiocyanate (1.2 ml). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was poured on to Bondesil 40 μM C8 resin (400 g) that had been prewashed with methanol (1 L) and water (1 L). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) followed by 20% acetonitrile in water (800 ml). Evaporation of the methanol gave compound BB as a yellow solid (7.3 g). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) Evaporation of the methanol
ソース ID: ord-bc301b1918944d069b746bb6779c014c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of compound AA (9.1 g) in dry N,N′-dimethylformamide (15 ml) was added n-decylisothiocyanate (1.2 ml). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was poured on to Bondesil 40 μM C8 resin (400 g) that had been prewashed with methanol (1 L) and water (1 L). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) followed by 20% acetonitrile in water (800 ml). Evaporation of the methanol gave compound BB as a yellow solid (7.3 g). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) Evaporation of the methanol
ソース ID: ord-bc301b1918944d069b746bb6779c014c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Procedure (12.) was employed with 1-formyl-2-(4-aminophenyl)hydrazine (1.51 g, 0.01 mole) and decyl isothiocyanate (1.99 g, 0.01 mole). Yield 2.4 g (69%), m.p. 150°-152° C.
ソース ID: ord-110174156d9a46cea1daf18641800ffb反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Procedure (12.) was employed with 1-formyl-2-(4-aminophenyl)hydrazine (1.51 g, 0.01 mole) and decyl isothiocyanate (1.99 g, 0.01 mole). Yield 2.4 g (69%), m.p. 150°-152° C.
ソース ID: ord-110174156d9a46cea1daf18641800ffb反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-787b95fd05694948bb9e0eecd8a1d368反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of compound AA (9.1 g) in dry N,N′-dimethylformamide (15 ml) was added n-decylisothiocyanate (1.2 ml). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was poured on to Bondesil 40 μM C8 resin (400 g) that had been prewashed with methanol (1 L) and water (1 L). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) followed by 20% acetonitrile in water (800 ml). Evaporation of the methanol gave compound BB as a yellow solid (7.3 g). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) Evaporation of the methanol
ソース ID: ord-efc564ca20644543b396101ebb2cd497反応条件: temp:85.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 0.511 G. of 4-Chloro-2-pyridyl isothiocyanate and 1.8 g. of n-decylisothiocyanate are combined and heated at 85° C. for 20 hours. The temperature is lowered to 75° C. and continued for 8 days. The reaction mixture is cooled, triturated with ether, filtered, washed with water and dried affording 8-chloro 3-(n-decyl) pyrido (1,2-a) 1,3,5-triazine-2,4-dithione m.p. 153°-155° C. is lowered to 75° C. The reaction mixture is cooled triturated with ether filtered washed with water dried
ソース ID: ord-e28dbc71cf6e40518f37c7328ca7a664反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of compound AA (9.1 g) in dry N,N′-dimethylformamide (15 ml) was added n-decylisothiocyanate (1.2 ml). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was poured on to Bondesil 40 μM C8 resin (400 g) that had been prewashed with methanol (1 L) and water (1 L). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) followed by 20% acetonitrile in water (800 ml). Evaporation of the methanol gave compound BB as a yellow solid (7.3 g). The product was eluted with methanol (800 ml) after being first washed with water (800 ml) Evaporation of the methanol
ソース ID: ord-bc301b1918944d069b746bb6779c014c反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Procedure (12.) was employed with 1-formyl-2-(4-aminophenyl)hydrazine (1.51 g, 0.01 mole) and decyl isothiocyanate (1.99 g, 0.01 mole). Yield 2.4 g (69%), m.p. 150°-152° C.
ソース ID: ord-110174156d9a46cea1daf18641800ffbPubChem 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。
