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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantTriethylamineHCID 8471—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantTert-butyl 3-formylmorpholine-4-carboxylateHCID 22342783—
SolventSodium HydroxideHCID 14798—
Product4-Boc-3-(2-carboxy-ethyl)-morpholineHCID 5342504240.3%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340538B2
Source datasetuspto-grants-2016_05
ORD IDord-5a06b252f6b54bf4ada29a6f44e92503
Source noteuspto-grants-2016_05