HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524579Generated: October 31, 2026
Formic Acid → 4-Boc-3-(2-carboxy-ethyl)-morpholine
https://huagongshe.com/reaction/524579
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Reactant | Tert-butyl 3-formylmorpholine-4-carboxylate | HCID 22342783 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Boc-3-(2-carboxy-ethyl)-morpholine | HCID 53425042 | 40.3% |
Reaction Steps
A mixture of formic acid (2.26 mL, 58.9 mmol) and triethylamine (3.36 mL, 24.11 mmol) was stirred for 5 minutes in an ice bath. To the mixture were added tert-butyl 3-formylmorpholine-4-carboxylate (0.47 g, 2.2 mmol) and Meldrum's acid (0.32 g, 2.2 mmol) in turn at 0° C. The reaction mixture was heated at 100° C. for 5 hours, and cooled down in an ice bath. To the resulting mixture was added aqueous NaOH solution (2 mol/L, 40 mL). The aqueous layer was extracted with EtOAc (50 mL×3) and the organic layer was discarded. To the aqueous layer was added EtOAc (80 mL), and the mixture was adjusted to pH 4-5 with HCl (1 mol/L) under stirring. The aqueous layer was extracted with EtOAc (80 mL). The organic layer was dried over anhydrous Na2SO4, then filtered and the filtrate was concentrated in vacuo to give the title compound as a white solid (0.23 g, 40%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340538B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-5a06b252f6b54bf4ada29a6f44e92503 |
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| Source note | uspto-grants-2016_05 |
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