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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956697Generated: November 2, 2026

Triethylamine → HCID 70199112, compound

https://huagongshe.com/reaction/1956697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 67642996HCID 67642996—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 70199112HCID 7019911219.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the product from Step G (63 mg, 0.17 mmol) in 2.5 mL of THF at 0° C. was added triethylamine (0.15 mL, 1.0 mmol), followed by triphosgene (31 mg, 0.10 mmol). The reaction was stirred at 0° C. for 1.5 hour, then poured into EtOAc and washed with sat. aq. NaHCO3 and brine. The solution was dried (Na2SO4), filtered, and concentrated in vacuo. The product was taken up in methanol and injected onto a preparative HPLC column and purified with a mixed gradient of 25%-55% acetonitrile/0.1% TFA; 75%-45% 0.1% aqueous TFA over 50 minutes. After concentration in vacuo, the resultant product was partitioned between dichloromethane and aq. NaHCO3 soln., and the aqueous phase was extracted with CH2Cl2. The organic solution was washed with brine, dried (Na2SO4), filtered, and concentrated to dryness to provide the product free base, which was taken up in CH2Cl2 and treated with excess 1M HCl/ether solution. After concentrated in vacuo, the titled product (9.3 mg) was isolated as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780492
Source datasetuspto-grants-1998_07
ORD IDord-bcba43788ce7499faae1927deeb2ded2
Source noteuspto-grants-1998_07