HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514632Generated: October 29, 2026
Hydrochloric Acid → Diethyl 2-(2-benzyloxyethyl)-2-hydroxymethylmalonate
https://huagongshe.com/reaction/514632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Diethyl 2-(2-(benzyloxy)ethyl)malonate | HCID 12549951 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Diethyl 2-(2-benzyloxyethyl)-2-hydroxymethylmalonate | HCID 67779176 | 90.6% |
Reaction Steps
2.85 g (9.67 mmol equivalents) of diethyl 2-(2-benzyloxyethyl)malonate was dissolved in 20 mL of acetonitrile, 1.60 g (11.7 mmol equivalents) of potassium bicarbonate and 465 mg (11.7 mmol equivalents as formaldehyde) of paraformaldehyde were added thereto, and the mixture was stirred at room temperature (25° C.) overnight. After completion of the reaction, a 0.5 mol/L aqueous solution of hydrochloric acid was added dropwise to the reaction liquid, and the mixture was extracted three times with chloroform. The combined chloroform layers were dried with anhydrous magnesium sulfate and then concentrated under vacuum, and the obtained crude product was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (v/v)=4/1) to give 2.78 g (8.76 mmol equivalents) of diethyl 2-(2-benzyloxyethyl)-2-hydroxymethylmalonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09107964B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-9878d03cb2334e3bbe1aaa2241202dc5 |
|---|
| Source note | uspto-grants-2015_08 |
|---|