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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119167Generated: November 2, 2026

N,N-Diethylaniline → HCID 13960862, compound

https://huagongshe.com/reaction/2119167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DiethylanilineHCID 7061—
ReactantPropylparabenHCID 7175—
ReactantDiphosgeneHCID 10426—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20191099HCID 20191099—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 13960862HCID 1396086235.5%

Reaction Steps

A solution of 250 mg (1.35 millimole) of n-propyl-p-hydroxybenzoate in 7 ml of THF was added to a solution of 0.12 ml (1.00 millimole) of trichloromethyl chloroformate in 2 ml of THF and then a solution of 0.25 ml (1.57 millimole) of N,N-diethylaniline in 6 ml of THF was added dropwise. The reaction mixture was stirred for 1.5 hrs at room temperature. Independently, 0.30 g (6.25 millimole) of sodium hydride washed with hexane was suspended in 5 ml of THF and a solution of 200 mg (0.63 millimole) of 5-isopropyloxycarbonyl-2,6-dimethyl-4-(2-nitrophenyl)-dihydropyrimidine in 5 ml os THF was added dropwise and stirred for 40 minutes at room temperature. And to this mixture the above reaction mixture was added and stirred for 30 minutes. Ice water was added and the mixture was extracted three times with ether. The organic layer was washed twice with water, dried over magnesium sulfate (dehydrating agent) and concentrated under reduced pressure. The residue was purified on silica gel by column chromatography (silica gel 30 g, eluant:benzene/ethyl acetate 9:1) to obtain 117 mg (35% yield) of tilte compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04683234
Source datasetuspto-grants-1987_07
ORD IDord-c5be33abbc5f4bb19e953eb2e087e38c
Source noteuspto-grants-1987_07