HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221315Generated: November 3, 2026
4-Methylmorpholine → HCID 13828186, compound
https://huagongshe.com/reaction/2221315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Reactant | methyl L-prolinate hydrochloride | HCID 2733200 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13828186 | HCID 13828186 | — |
Reaction Steps
Boc-Val-OH (3.00 g, 13.8 mmol) was dissolved in 10 ml of dry THF and cooled down to −15° C. To the mixture CAIBE (1.80 ml, 13.8 mmol) and NMM (1.52 ml, 13.8 mmol) where added and the solution was stirred until the formation of the mixed anhydride was complete. Then the mixture was brought to −10° C. and NMM (1.52 ml, 13.8 mmol) was added followed by H-Pro-OMe.HCl (2.29 g, 13.8 mmol). The mixture was allowed to reach room temperature and left overnight. After removing the solvent and the usual workup the resulting ester 1 was taken without further characterisation. The ester 1 was dissolved in HCl/HOAc (5 ml, 6N) and left at 0° C. until the removal of the Boc-group was complete. The solvent was then removed and the resulting oil was treated with diethylether to give a white solid 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368576B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-581463bc495445dbb0155c72b87fe0d1 |
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| Source note | uspto-grants-2008_05 |
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