HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271659Generated: November 2, 2026
Alanine methyl ester hydrochloride → HCID 87830865, compound
https://huagongshe.com/reaction/1271659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Alanine methyl ester hydrochloride | HCID 2733257 | — |
| Reactant | Hydroxybenzenesulfonic acid | HCID 15619088 | — |
| Solvent | Methyl Acetate | HCID 6584 | — |
| Product | HCID 87830865 | HCID 87830865 | — |
Reaction Steps
L-Ala-OMe HCl salt (1.00 g, 7.16 mmol) was suspended in methyl acetate (15 ml), and benzenesulfonic acid monohydrate (BsOH H2O) (1.51 g, 8.57 mmol) was added. The mixture was stirred for dissolution. This solution was concentrated under reduced pressure, and methyl acetate (15 ml) was added. The mixture was concentrated twice under reduced pressure, and the obtained concentrate was cooled in a refrigerator. Since partial crystallization occurred, diethyl ether (3 ml) and methyl acetate (15 ml) were added to dissolve the crystals almost entirely at 40° C. This solution was stirred at room temperature and cooled overnight in a refrigerator. The crystals were separated and dried to give L-alanine methyl ester benzenesulfonate (L-Ala-OMe BsOH salt) crystals. The crystals were left standing at room temperature for a while. As a result, the crystals were liquefied and failed to provide stable crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07205433B2 |
|---|
| Source dataset | uspto-grants-2007_04 |
|---|
| ORD ID | ord-a6c4c991277f457bb6108fd023fea4c5 |
|---|
| Source note | uspto-grants-2007_04 |
|---|