HuagongsheHuagongshe Chemistry Print Report · For research reference only
Naphthalene → 2-Hydroxy-but-3-enoic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Naphthalene | HCID 931 | — |
| Reactant | Sucrose | HCID 5988 | — |
| Reactant | Ethyl Lactate | HCID 7344 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Hydroxy-but-3-enoic acid ethyl ester | HCID 13271482 | 48% |
Reaction Conditions
| Temperature | 160 °C |
|---|
Reaction Steps
An autoclave (50 cc microclave) is charged with 8.0 g of ethanol, 0.2252 g of sucrose (0.6578 mmol), 118.9 mg naphthalene (internal standard) and finally with 160.0 mg Sn-BEA (prepared according to U.S. Pat. No. 6,306,364). The autoclave is closed, charged with 20 bar of argon and heated to 160° C. After the temperature reaches 100° C., the mechanical stirrer is started (500 rpm) and the mixture is heated for 20 hours under these conditions. GC-analysis of the reaction mixture shows that 1.03 mmol of ethyl lactate is formed (39%) together with 0.316 mmol ethyl 2-hydroxy-3-butenoate (16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143439B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-c107c959140b4e37a91e2c840f1f3d4f |
| Source note | uspto-grants-2012_03 |