HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523853Generated: October 31, 2026
Palmitoyl Serinol → HCID 42606463, compound
https://huagongshe.com/reaction/523853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Palmitoyl Serinol | HCID 9862307 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 42606463 | HCID 42606463 | — |
Reaction Steps
1.0 g. of the resulted 2-(hexadecanoylamino)propane-1,3-diol were transferred to a three necks round bottom flask equipped with a dropping funnel, a cooling bath, and a magnetic stirrer, under an air stream. The compound was dissolved in 200 ml dry THF and the solution wasp cooled to 0° C. 1.2 g of LiAlH4 were added in small portions with strong stirring during 1 hour and then the mixture was left to react for another 2 hours at 0° C. The cooling bath was removed and the reaction was left to stir overnight. The next day, 2 ml of ethyl acetate followed by 10 ml of methanol and 10 ml of HCl 1N, were added very slowly and the solution was evaporated to approximately 20 ml. The mixture was transferred to a separatory funnel and 100 ml water, 100 ml dichloromethane and 50 ml methanol were added. Following shaking, the lower phase was collected and the upper, acidic-aqueous-methanolic phase was extracted twice with 50 ml CH2Cl2:MeOH, 3:1. The combined organic phases were washed with 100 ml HCl 0.1 N and then with 100 ml H2O, dried for 2 hours over MgSO4, filtered and evaporated to dryness. The resulted product was crystallized from ethanol:H2O. Yield: 0.5 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09340488B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-272df5e46e5e43c2931dc636a2bdc3da |
|---|
| Source note | uspto-grants-2016_05 |
|---|