Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256544Generated: October 30, 2026

Hydrochloric Acid → HCID 86747346, compound

https://huagongshe.com/reaction/256544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantHexamethylphosphorous triamideHCID 15355—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67857954HCID 67857954—
ReactantHCID 178418689HCID 178418689—
SolventBenzeneHCID 241—
ProductHCID 86747346HCID 8674734646%

Reaction Steps

This reaction was performed in a dry box under N2 (10% relative humidity). A suspension of 0.228 g (0.908 mmol) of 9 in 10 mL of benzene was added in 0.5 mL portions over 20 min to a solution of 0.45 mL (1.36 mmol) of MeMgBr (3.0M in Et2O) in 10 mL of benzene. The mixture was stirred at room temperature for 30 min. A solution of 0.243 g (1.36 mmol) of hexamethylphosphorous triamide in 1 mL of benzene was added. The mixture was stirred for 15 min, then a suspension of 0.273 g (9.08 mmol) of paraformaldehyde in 2 mL of benzene was added. The mixture was heated under reflux for 4 h, cooled, and transferred to a 1 L beaker. Two hundred milliliters of 5% HCl was added and the resulting mixture was stirred for 10 min. The mixture was made basic with solid NaHCO3 and was extracted with 100 mL of Et2O, then with four 75 mL portions of CHCl3. The combined extracts were dried (Na2SO4) and volatiles were removed under reduced pressure to produce a green oil which was converted into its HCl salt with ethereal HCl. The salt was washed with two 5 mL portions of abs EtOH to give 0.130 g (46%) of a white solid, mp 255°-258° C. (decomp). Lit1 mp of (R) enantiomer 260°-262° C. (decomp).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258384
Source datasetuspto-grants-1993_11
ORD IDord-42830d3ab3ff4bd8bb051f4b717cd0e2
Source noteuspto-grants-1993_11