HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butoxy-4-formyl-benzoic Acid Methyl Ester → 2-Butoxy-4-({[4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-benzoic Acid Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butoxy-4-formyl-benzoic Acid Methyl Ester | HCID 57443319 | — |
| Reactant | 4-[(tert-butyldimethylsilyl)oxy]-N,2-dimethylaniline | HCID 66704120 | — |
| Reactant | 4-({[4-(Tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-2-methyl-benzoic acid methyl ester | HCID 66704169 | — |
| Product | 2-Butoxy-4-({[4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-benzoic Acid Methyl Ester | HCID 66704181 | — |
Reaction Steps
The title compound is prepared by reductive amination of [4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amine with 2-butoxy-4-formyl-benzoic acid methyl ester, essentially as described in the synthesis of 4-({[4-(tert-butyl-dimethyl-silanyloxy)-2-methyl-phenyl]-methyl-amino}-methyl)-2-methyl-benzoic acid methyl ester using the appropriate starting material. The title compound is obtained as syrup after workup. LC-ES/MS m/e 472.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106077B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-0d21f20779364c87894f4c8590f3927a |
| Source note | uspto-grants-2012_01 |