反应 #4059403
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-4d0b436ff98d453ba0bfabc7d69c291e暂无可渲染的结构数据
C1COC2=C(C1O)C=C(C=C2)F产品信息
6-氟-3,4-二氢-2H-色烯-4-醇(CAS 457628-46-5)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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合成路线数据
10 条反应 · 10 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4d0b436ff98d453ba0bfabc7d69c291e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acidn (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-751b6c69702f43e4a75192feda8c9bea反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acid (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-f522847bc1fe43028b8ad6d304a02838反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acid (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-f522847bc1fe43028b8ad6d304a02838反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4d0b436ff98d453ba0bfabc7d69c291e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acidn (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. 29c) +/−cis-6-Fluoro-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl ester The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-d01cedc1825b43618f2e445d90c31b96反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acid (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-084dcb2372cc4ad49d7e3df4f18ffff9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acidn (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-ed476416adfa43ef88d97ed98cbb7a69反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acidn (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-751b6c69702f43e4a75192feda8c9bea反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 6-Fluorochroman-4-ol (8 g, 48 mmol) and toluene-4-sulphonic acid (1 g) were dissolved in toluene and refluxed over-night with subsequent water removal. The mixture was then cooled and washed with NaHCO3 (aq) and purified by chromatography (silica gel, n-hexane) to give 4.2 g (52%) of pure 6-fluoro-2H-chromene. The mixture was then cooled washed with NaHCO3 (aq) purified by chromatography (silica gel, n-hexane)
来源 ID: ord-f522847bc1fe43028b8ad6d304a02838PubChem References
以下资料来自该化合物的公开数据库参考记录。
