Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15480970 | HCID 15480970 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9841928 | HCID 9841928 | — |
Reaction Steps
L-alanine laurylamide (2.5 g) and 1 g of sodium hydroxide were dissolved in 20 ml of methanol, and 1.0 ml of salicylaldehyde and 0.1 g of sodium borohydride were added thereto in this order. After the mixture was stirred for 1 hour, 1.0 ml of salicylaldehyde and 0.1 g of sodium borohydride were added thereto again in this order. The mixture was stirred overnight at room temperature, and the insoluble matter was then separated through filtration. The filtrate was adjusted to a pH of 7 with hydrochloric acid, and concentrated under reduced pressure. The resulting oil was dissolved in diethyl ether, washed with water, and then dried over with magnesium sulfate. After the drying agent was separated through filtration, the filtrate was concentrated under reduced pressure to give 3 g of N-(2-hydroxybenzyl)-L-alanine laurylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05985922 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-7729b823018c47ff9114913af103bdfc |
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| Source note | uspto-grants-1999_11 |
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