HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680594Generated: November 2, 2026
Hydrochloric Acid → O-methyl homoserine methyl ester hydrochloride
https://huagongshe.com/reaction/1680594
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | (S)-2-amino-4-methoxybutanoic acid | HCID 447570 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | O-methyl homoserine methyl ester hydrochloride | HCID 86737808 | — |
Reaction Steps
A solution of 13.3 g of O-methyl homoserine in 370 ml of methanol and 180 ml of a 6 N solution of hydrogen chloride in dioxane is allowed to stand at room temperature for 3 to 4 days. The solvent is removed under reduced pressure and the residue lyophilized to give O-methyl homoserine methyl ester hydrochloride which is represented by the following formula ##STR51## Substitution of an equivalent quantity of O-methyl homoserine methyl ester hydrochloride for the methyl D-methioninate hydrochloride of Example 35 and substantial repetition of the procedures described in Examples 35 through 39 provides methyl DL-2,6-dimethyltyrosyl-DL-O-methylhomoseryl-glycyl-L-phenylalanyl-3-amino-1-adamantanecarboxylate hydrochloride which is represented by the following formula ##STR52##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04273704 |
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| Source dataset | uspto-grants-1981_06 |
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| ORD ID | ord-086fd2fd23d74d2ea8e3c8cd67d5a83c |
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| Source note | uspto-grants-1981_06 |
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