反应 #4163425
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-17cf3ee1ae6544c2b21f8225a23bcc86暂无可渲染的结构数据
CCCCCC(=O)[O-]产品信息
己酸甲酯(CAS 151-33-7)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
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-17cf3ee1ae6544c2b21f8225a23bcc86反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4cf4865d407e483bbb5560ea16b5db17反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-86a5c4763b774f8996f3b078b92d846e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to that set forth in A, but substituting for acetic anhydride, the anhydrides or halides of propionic, butanoic, pentanoic, or hexanoic acid, the corresponding manoalide δ-lactone propionate, butanoate, pentanoate, and hexanoate are prepared.
来源 ID: ord-49c4915b85f541c69ec86d494d307485反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This dione was prepared by the acid cyclization of ethyl 6-(3'chlorophenyl)-6-cyano-5-keto-3,3-dimethylhexanoate. Preparation of the hexanoate is described in Part A and of the dione in Part B below.
来源 ID: ord-dae522f735ba49fbb213c222fedb8f48反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This dione was prepared by acid cyclization of ethyl 6-(4'methylphenyl)-6-cyano-5-keto-3,3-dimethylhexanoate. Preparation of the hexanoate is described in Part A and of the dione in Part B.
来源 ID: ord-5fb7c0ed54084c08a58aa9755be44477反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-17cf3ee1ae6544c2b21f8225a23bcc86反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to that set forth in A, but substituting for acetic anhydride, the anhydrides or halides of propionic, butanoic, pentanoic, or hexanoic acid, the corresponding manoalide δ-lactone propionate, butanoate, pentanoate, and hexanoate are prepared.
来源 ID: ord-49c4915b85f541c69ec86d494d307485反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This dione was prepared by the acid cyclization of ethyl 6-(3'chlorophenyl)-6-cyano-5-keto-3,3-dimethylhexanoate. Preparation of the hexanoate is described in Part A and of the dione in Part B below.
来源 ID: ord-dae522f735ba49fbb213c222fedb8f48反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This dione was prepared by acid cyclization of ethyl 6-(4'methylphenyl)-6-cyano-5-keto-3,3-dimethylhexanoate. Preparation of the hexanoate is described in Part A and of the dione in Part B.
来源 ID: ord-5fb7c0ed54084c08a58aa9755be44477反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This dione was prepared by acid cyclization of ethyl 6-(4'methylphenyl)-6-cyano-5-keto-3,3-dimethylhexanoate. Preparation of the hexanoate is described in Part A and of the dione in Part B.
来源 ID: ord-5fb7c0ed54084c08a58aa9755be44477反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4cf4865d407e483bbb5560ea16b5db17PubChem References
以下资料来自该化合物的公开数据库参考记录。
