反应 #4161391
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-fc8aa0539d5048d4b5045a5f2c4c4d20暂无可渲染的结构数据
C(C(Cl)Cl)O产品信息
2,2-二氯乙醇(CAS 598-38-9)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
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fc8aa0539d5048d4b5045a5f2c4c4d20反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fc8aa0539d5048d4b5045a5f2c4c4d20反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using the procedure of Step F of Example 9, 4.8 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-hydroxy-3-oxo-1-propenyl]-cyclopropane-carboxylate and 2 ml of 2,2-dichloroethanol were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate. were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate
来源 ID: ord-f73adc060403419eaa4b4558531b1d7d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using the procedure of Step F of Example 9, 4.8 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-hydroxy-3-oxo-1-propenyl]-cyclopropane-carboxylate and 2 ml of 2,2-dichloroethanol were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate. were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate
来源 ID: ord-f73adc060403419eaa4b4558531b1d7d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using the procedure of Step F of Example 9, 4.8 g of tert.-butyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-hydroxy-3-oxo-1-propenyl]-cyclopropane-carboxylate and 2 ml of 2,2-dichloroethanol were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate. were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate
来源 ID: ord-37049aa871b641ee8f72360e4e35eb1c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using the procedure of Step F of Example 9, 4.8 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-hydroxy-3-oxo-1-propenyl]-cyclopropane-carboxylate and 2 ml of 2,2-dichloroethanol were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate. were reacted to obtain after elution with a 9-1 mixture of cyclohexane-ethyl acetate 5.6 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-dichloroethoxy)-1-propenyl]-cyclopropane-carboxylate
来源 ID: ord-f73adc060403419eaa4b4558531b1d7dPubChem References
以下资料来自该化合物的公开数据库参考记录。
