反応 #4122797
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-e0b711780e5c40c888387a173e6ccad2表示可能な構造データがありません
CCC1=CC=CC=C1O製品情報
2-ethylphenol (CAS 90-00-6) 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 6997
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-e0b711780e5c40c888387a173e6ccad2反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-65ae74334fe5444e81a382b0f50e3632反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-04d9c3ab64bc430fa7c403d882575bc9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8fb75896a31e46eca939266bfd95349a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-7d307a1475f4410397d343f325b24899反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3684210410494d15872cc468283b410e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-08faa21611874714818bb8f4348b33df反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-3b465757d64f4c9ba18c27cb7799d607反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c9ee31c05b1f42faa28a1ee897ee7ee7反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9fa17b0025ee4ccabbbe6e2460cb9f0a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9712c566edac42b58063b57bea932e90反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 2-ethylphenol (2.44 g, 20 mmol) in 80 mL of anhydrous acetonitrile was treated with nitronium tetrafluoroborate (2.93 g, 22 mmols) in portions over a period of 5 minutes at −30° C. to −40° C. After 20 minutes, the mixture was quenched with ice, treated with cold water and extracted with three 100 mL portions of dichloromethane. The combined organic layers were washed with two 30 mL portions of water, dried over sodium sulfate, filtered, and concentrated in vacuo. Chromatography on SiO2 (20% ethyl acetate in hexanes) gave 2.0 g of 2-ethyl-6-nitrophenol as a yellow oil (60% yield). the mixture was quenched with ice treated with cold water extracted with three 100 mL portions of dichloromethane The combined organic layers were washed with two 30 mL portions of water dried over sodium sulfate filtered concentrated in vacuo
ソース ID: ord-9ba1b52adac64ee2b33689d216471ae9PubChem 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。
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