HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl Benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Phenylglyoxylonitrile | HCID 11953 | — |
| Product | Methyl Benzoate | HCID 7150 | — |
Reaction Steps
For example, when pure benzoyl cyanide (i.e., containing essentially no halide ion or halide ion source, such as benzoyl chloride) is reacted with concentrated sulfuric acid and then esterified by further reaction with methanol, the cyano group is cleaved and methyl benzoate is formed as follows: ##STR2##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04234739 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-3210b225ed214befa775d9f51e527f56 |
| Source note | uspto-grants-1980_11 |