反应 #4141531
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-4cac3f06b264485681ff99b35cbfbd48暂无可渲染的结构数据
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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-4cac3f06b264485681ff99b35cbfbd48反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ce4c9e5e6b6a41ea83903d7434ffd21c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9a601264f22a4d62b71badc5e3a23481反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5fd2330d0db64019ab881049c835cd26反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b24c6ed39ee943ce8241c6989eeab692反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-19074fe68389431da717e3d8de85e0c2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 10 mmol of ethyl acrylate, 50 mmol of adamantane, 1 mmol of N-hydroxyphthalimide, 0.01 mmol of cobalt(II) acetate, 0.1 mmol of acetylacetonatocobalt(III), and 54 mmol of acetonitrile was stirred at 70° C. in an oxygen atmosphere (1 atm) for 8 hours. A reaction mixture was concentrated, and the concentrate was subjected to column chromatography on a silica gel to yield ethyl 3-(adamant-1-yl)-2-hydroxypropionate of the following formula (a), ethyl 3-(adamant-1-yl)-2-oxopropionate of the following formula (b), and ethyl 1-adamantaneacetate of the following formula (c) in yields of 55%, 16%, and 8%, respectively. The conversion rate from ethyl acrylate was 99%. A reaction mixture was concentrated
来源 ID: ord-3faca7f0bfd44f1293e90cc3d06b9481反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Aluminum trichloride (40 g, 3 mol) was added slowly to thionyl chloride (200 ml, 2.7 mol), and the mixture was cooled to -20°. Adamantane was added in portions over 21/2 hrs, and the resulting mixture was stirred 1 hr and allowed to warm to room temperature. After the thionyl chloride was removed under vacuum, the residue was diluted with CCl4 ; and the aluminum trichloride was decomposed with ice and water. The layers were separated; and the organic layer was washed (brine), dried (Na2SO4), filtered, and concentrated under vacuum. The residue was distilled under vacuum (1 torr, 133.3 Pascals) with a vigreaux column to give the product (28.8 g; bp 118°-128°) as a waxy solid; TLC, Rf =0.6-0.4, EtOAc:hexanes (15:85). the mixture was cooled to -20° After the thionyl chloride was removed under vacuum the residue was diluted with CCl4 The layers were separated and the organic layer was washed (brine) dried (Na2SO4) filtered concentrated under vacuum The residue was distilled under vacuum (1 torr, 133.3 Pascals) with a vigreaux column to give the product (28.8 g; bp 118°-128°) as a waxy solid
来源 ID: ord-dc4ffeb8e0ef4ff193419b458a06d83d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4cac3f06b264485681ff99b35cbfbd48反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4cac3f06b264485681ff99b35cbfbd48反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction of catechol with 1,3-adamantane-diol according to the method described by Lu et al (Lu et al. J Med Chem 2005, 48 (14), 4576-4585) gave the adduct 10 in reasonable yield.
来源 ID: ord-aed952d387894b8fbb04f8c20887eaaf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Reaction of catechol with 1,3-adamantane-diol according to the method described by Lu et al (Lu et al. J Med Chem 2005, 48 (14), 4576-4585) gave the adduct 10 in reasonable yield.
来源 ID: ord-aed952d387894b8fbb04f8c20887eaafPubChem References
以下资料来自该化合物的公开数据库参考记录。
