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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261438Generated: October 27, 2026

Hydrochloric Acid → HCID 59608829, compound

https://huagongshe.com/reaction/1261438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantAmmonium ChlorideHCID 25517—
ReactantTriphosgeneHCID 94429—
ReactantSodium BicarbonateHCID 516892—
ReactantAcetone cardiceHCID 18522661—
ReactantEthyl 3-hydroxy-2-(hydroxymethyl)-2-methylpropanoateHCID 23370761—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 59608829HCID 59608829112.8%

Reaction Steps

A solution of triphosgene (19.5 g, 0.065 mol) in CH2Cl2 (200 mL) was added stepwise to a CH2Cl2 solution (150 mL) of ethyl 2,2-bis(methylol)propionate (MPAEt) (21.1 g, 0.131 mol) and pyridine (64 mL, 0.786 mol) over 30 min at −75° C. with dry ice/acetone. The reaction mixture was kept stirring for another 2 hours under chilled condition and then allowed to heat to room temperature. Saturated NH4Cl aqueous solution (200 mL) was added to the reaction mixture to decompose excess triphosgene. The organic phase was then treated with 1 N HCl aq (200 mL), followed by saturated NaHCO3 (200 mL), brine (200 mL), and water (200 mL). After the CH2Cl2 solution was dried over MgSO4 and evaporated, the residue was recrystallized from ethylacetate to give white crystals (13.8 g, 56%). 1H NMR: delta 4.68 (d, 2H, CH2OCOO), 4.25 (q, 1H, OCH2CH3), 4.19 (d, 2H, CH2OCOO), 1.32 (s, 3H, CH3), 1.29 (t, 3H, CH3CH2O). 13C NMR: delta 171.0, 147.5, 72.9, 62.1, 39.9, 17.3, 13.8. HR-ESI-MS: m/z calcd for C8H12O5.Na, 211.0582; found, 221.0578.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470891B2
Source datasetuspto-grants-2013_06
ORD IDord-21b9504a3a6e4da0bb1b38931714e096
Source noteuspto-grants-2013_06