反应 #4163374
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-44b7d4a8734a4f37a51820160b13c561暂无可渲染的结构数据
CC(C)(C)C1=CC=CC=C1O产品信息
2-叔丁基苯酚(CAS 88-18-6)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 6923
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-44b7d4a8734a4f37a51820160b13c561反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-25cf2bfb919a4811b3812d6b39c77e99反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b052f3abafbf45ec851b3dcab61549d8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c556a74936d7458fbea97131eba24026反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4e8dc345f0da4cc8b715c7645f09ce42反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a1f2fa122569498d99943c1f9519f0f6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-efae10bd98e24efb962eddeb303941c4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1adc34d1f4b042bda42cb19c99e012f2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-01f35470be85485897e65ed83ca0dd9a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4388f85122cb4bc6a82c6c4562f597b9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-tert-butylphenol (250 g, 1.67 mol) in CH3CN (1500 mL) was added NBS (300 g, 1.67 mol) at room temperature. After addition, the mixture was stirred at room temperature overnight and then the solvent was removed. Petroleum ether (1000 mL) was added, and the resulting white precipitate was filtered off. The filtrate was concentrated under reduced pressure to give the crude 2-tert-butyl-4-bromophenol (380 g), which was used without further purification. After addition the solvent was removed Petroleum ether (1000 mL) was added the resulting white precipitate was filtered off The filtrate was concentrated under reduced pressure
来源 ID: ord-94c93ce486b5457da7695c4b2b7cdb86反应条件: temp:-45.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a dry, round bottom flask was added aluminum chloride (4.402 g, 33.0 mmol). The flask was then cooled to −45° C. After 10 minutes, dry toluene (80 mL) was added followed by dropwise addition of 2-tert-butylphenol (5.00 mL, 32.7 mmol) (commercially available from Sigma-Aldrich, St. Louis, Mo., USA). The mixture was stirred and maintained at −4° C. After 1.5 hours, acetyl chloride (2.40 mL, 33.8 mmol) was carefully added dropwise. The mixture was allowed to warm to room temperature and monitored with TLC and LC-MS. After 18 hours, the mixture was slowly poured onto crushed ice. This mixture was stirred at room temperature and the crystals were collected by filtration. The light yellow solid was identified as T17.1 (4.2589 g, 68%). MS ESI (pos.) m/e: 193.1 (M+H)+. maintained at −4° C After 1.5 hours to warm to room temperature After 18 hours the mixture was slowly poured onto crushed ice This mixture was stirred at room temperature the crystals were collected by filtration
来源 ID: ord-79d1bc3808f145d7a76551d7208413c7PubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 88-69-7
CAS 91967-91-8
CAS 90-68-6
CAS 79-96-9
CAS 4151-60-4
CAS 81910-71-6
CAS 96-65-1
CAS 2772-45-4
CAS 79-97-0
CAS 499-75-2
CAS 5875-45-6
CAS 23504-03-2
