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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452780Generated: October 31, 2026

4-Nitrophenethyl alcohol → HCID 18765769, compound

https://huagongshe.com/reaction/1452780

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenethyl alcoholHCID 7494—
ReactantTriethylamineHCID 8471—
ReactantTributylphosphineHCID 13831—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Phenyl-1,2,3,6-tetrahydropyridine hydrochlorideHCID 2723860—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventDichloromethaneHCID 6344—
ProductHCID 18765769HCID 1876576965.1%

Reaction Conditions

Temperature23 °C

Reaction Steps

1.29 g (6.6 mmole) of 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride, 0.92 ml (6.6 mmole) of Et3N and 1.62 ml (6.6 mmole) of tributylphosphine are added to a solution of 1.0 g (5.98 mmole) of 4-nitrophenethyl alcohol in 25 ml of CH2Cl2. The reaction mixture is agitated vigorously at 23° C. and 1.04 ml (6.6 mmole) of diethylazodicarboxylate is added dropwise. After 4 hours, the reaction is stopped by adding 5 ml of a saturated solution of NH4Cl. After decantation, the aqueous phase is extracted twice with 5 ml of CH2Cl2, the organic phases are combined and washed twice with 5 ml of water, twice with 5 ml of brine, dried over magnesium sulphate, filtered and concentrated under vacuum. The residue is purified on a silica column (eluent Heptane/AcOEt: 9/1 to 7/3) in order to produce 1.20 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473779B2
Source datasetuspto-grants-2009_01
ORD IDord-52b8b93ab60c4eb99d5ee304bbdf94bb
Source noteuspto-grants-2009_01