反应 #4045755
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-8e3b6daee5b04268a6c8986b0b43423f暂无可渲染的结构数据
C1C(CN1)OC2=CC=CC=C2C(F)(F)F产品信息
3-[2-(三氟甲基)苯氧基]氮杂环丁烷(CAS 76263-24-6)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。
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数据库编号 12812505
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合成路线数据
9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8e3b6daee5b04268a6c8986b0b43423f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The compound was prepared from 3-[2-(trifluoromethyl)phenoxy]azetidine and methylisocyanate as described in Example 5 of U.S. Pat. No. 4,226,861, m.p. 134°-136° C.
来源 ID: ord-305632c5062545c8bb586db723d8bc89反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirring solution of 3-(2-trifluoromethylphenoxy) azetidine (4.5 g., 0.02 mole) in 50 ml. of dry benzene was added slowly at room temperature 1.2 g. (0.02 mole) of methylisocyanate. After an additional 30 minutes a solid separated which was collected and recrystallized from benzene. The product (3.5 g., 68%) melted at 134°-136° C. After an additional 30 minutes a solid separated which was collected recrystallized from benzene
来源 ID: ord-6ab3cd699c274f039b258f156f05e8aa反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8e3b6daee5b04268a6c8986b0b43423f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 4.5 g (0.02 mole) of 3-[2-(trifluoromethyl)phenoxy]azetidine stirring in 50 ml of dry benzene, was added slowly 1.2 g (0.02 mole) of methyl isocyanate at room temperature. Stirring was continued for 30 minutes. A solid formed, and after filtration was recrystallized from benzene to yield 3.5 g (68%), mp 134°-136°. A solid formed after filtration was recrystallized from benzene to yield 3.5 g (68%), mp 134°-136°
来源 ID: ord-1a3a609d96214fbe9589953797d87e93反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The compound was prepared from 3-[2-(trifluoromethyl)phenoxy)azetidine and methylisocyanate as described in Example 5 of U.S. Pat. No. 4,226,861, m.p. 134°-136° C.
来源 ID: ord-c07ddac510a84c73b6590f0eb01af94c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The compound was prepared from 3-[2-(trifluoromethyl)phenoxy]azetidine and methylisocyanate as described in Example 5 of U.S. Pat. No. 4,226,861, m.p. 134°-136° C.
来源 ID: ord-2d58d4b099f049d99045a40a22b1af50反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The compound was prepared from 3-[2-(trifluoromethyl)phenoxy]azetidine and methylisocyanate as described in Example 5 of U.S. Pat. No. 4,226,861, m.p. 134°-136° C.
来源 ID: ord-305632c5062545c8bb586db723d8bc89反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirring solution of 3-(2-trifluoromethylphenoxy) azetidine (4.5 g., 0.02 mole) in 50 ml. of dry benzene was added slowly at room temperature 1.2 g. (0.02 mole) of methylisocyanate. After an additional 30 minutes a solid separated which was collected and recrystallized from benzene. The product (3.5 g., 68%) melted at 134°-136° C. After an additional 30 minutes a solid separated which was collected recrystallized from benzene
来源 ID: ord-6ab3cd699c274f039b258f156f05e8aaPubChem References
以下资料来自该化合物的公开数据库参考记录。
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