Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | D-Valine | HCID 71563 | — |
| Product | 3-Chlorobenzoic Acid | HCID 447 | — |
Reaction Steps
23.4 g (0.1 mol) of the Schiff base of D-valine and anisaldehyde prepared according to Ia) was dissolved, with stirring, in 130 ml of dry dichloromethane. The solution was cooled to 5° C. or lower. The stirring was continued and the temperature was allowed to rise to room temperature, after which the stirring was continued for 4 more hours. After about 0.5 hour's stirring at room temperature the mixture became turbid as a result of the crystallization of meta-chlorobenzoic acid. After the reaction, in which all the meta-chlorobenzoic acid formed crystallized, the reaction mixture was filtered and the filtered solution was evaporation until dry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05101036 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-7a172da08249415e978b824ed5381147 |
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| Source note | uspto-grants-1992_03 |
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