HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 2,4-dibromobutanoate → Diethyl 2-phenyl-3-cyano-6-chlorohexane-3,4-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 2,4-dibromobutanoate | HCID 296716 | — |
| Reactant | Ethyl 2-cyano-3-phenylbutyrate | HCID 11229687 | — |
| Reactant | Ethyl 2,4-dichlorobutanoate | HCID 12613704 | — |
| Reactant | Methyl 2-cyano-3-phenylbutyrate | HCID 13276234 | — |
| Product | Diethyl 2-phenyl-3-cyano-6-chlorohexane-3,4-dicarboxylate | HCID 20279787 | — |
Reaction Steps
Ethyl 2-cyano-3-phenylbutyrate and ethyl 2,4-dichlorbutyrate can be used in place of methyl 2-cyano-3-phenylbutyrate and methyl 2,4-dibromobutyrate, respectively, in the alkylation reaction of Example 3 to produce the corresponding diethyl 2-phenyl-3-cyano-6-chlorohexane-3,4-dicarboxylate. The latter product can then be reacted with the tricarboxylate of Example 4 and the dicarboxylate of Example 7 to give the corresponding pentaester and tetraester products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514340 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-25aa6375a4c54e6dbf924954e0ef406a |
| Source note | uspto-grants-1985_04 |