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HRID127893

反应详情

EQUATION

反应方程式

HRID 127893 的结构方程式

REACTANTS

反应物

6
结构：OCc1ccccc1
HCID244

Benzyl alcohol

C7H8O

结构：COc1ccc(CO)cc1
HCID7738

(4-Methoxyphenyl)methanol

C8H10O2

结构：OCC(Cl)(Cl)Cl
HCID8259

2,2,2-Trichloroethanol

C2H3Cl3O

结构：CC1(C)C2CCC1(C)C(O)C2
HCID64685

1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

C10H18O

结构：COC(=O)C1C(NC(=O)OCc2ccccc2)C(=O)N1Cc1ccc(OC)cc1OC
HCID13470810

未命名化合物

结构：COC(=O)C1C(NC(=O)OCc2ccc(OC)cc2)C(=O)N1Cc1ccc(OC)cc1OC
HCID23470086

未命名化合物

PRODUCTS

生成物

1
结构：COC(=O)C1C(NC(=O)OCC(Cl)(Cl)Cl)C(=O)N1Cc1ccc(OC)cc1OC
HCID14230565

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

1
结构：CC(C)(C)O
溶剂HCID6386

tert-Butyl alcohol

C4H10O

PROCEDURE

实验过程

When p-methoxybenzyl alcohol, isoborneol, benzyl alcohol, or 2,2,2-trichloroethanol is substituted for t-butanol in Example 3, methyl 3-(p-methoxybenzyloxycarbonylamino)-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate, methyl 3-(isobornyloxycarbonylamino)-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate, methyl 3-(benzyloxycarbonylamino)-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate, or methyl 3-(2,2,2-trichloroethoxycarbonylamino)-1-(2,4-dimethoxybenzyl)-4-oxoazetidine-2-carboxylate is obtained.