Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Alanine | HCID 5950 | — |
| Reactant | Hydroxybenzenesulfonic acid | HCID 15619088 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10401174 | HCID 10401174 | 163.6% |
Reaction Steps
L-alanine (1.50 g, 16.84 mmol) and benzenesulfonic acid monohydrate (BsOH H20) (3.56 g, 20.20 mmol) were added to ethanol (10 ml), and the mixture was heated overnight at 70° C. to perform esterification. To complete the esterification reaction, the mixture was heated to 90° C. and ethanol (200 ml) was added over 3.5 hours while distilling away almost the same amount of ethanol. Thereafter, the solvent was evaporated under reduced pressure, and the residue was dried under reduced pressure. Ethanol (0.5 ml) and diethyl ether (30 ml) were added to partially crystallize an oily residue, and the mixture was stirred at room temperature to give a slurry. This slurry was cooled overnight in a refrigerator, and the crystals were separated and dried to give 4.55 g of L-alanine ethyl ester benzenesulfonate (L-Ala-OEt BsOH salt) dry crystals (L-Ala-OEt BsOH salt content 87.6%, (14.47 mmol), yield 86.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205433B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-eb75df2a89614cd6822c4fa6f0b84328 |
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| Source note | uspto-grants-2007_04 |
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