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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418645Generated: October 30, 2026

Triphenylphosphine → HCID 58790022, compound

https://huagongshe.com/reaction/418645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-MorpholinoethanolHCID 61163—
ReactantDiethyl azodicarboxylateHCID 5462977—
ReactantHCID 136019957HCID 136019957—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58790022HCID 5879002279.1%

Reaction Steps

DEAD (0.96 mL, 6.07 mmol) was added to a solution of the compound 137 (1.78 g, 4.33 mmol), 2-morpholinoethanol (0.74 mL, 6.07 mmol) and triphenylphosphine (1.59 g, 6.07 mmol) in THF (43 mL). The reaction mixture was stirred at room temperature until completion of the reaction. The mixture was quenched with a saturated aqueous solution of ammonium chloride then extracted three times with ethyl acetate and 3 times with dichloromethane (with a bit of methanol inside). The combined organic layers were washed with water and brine, dried over anhydrous MgSO4, filtered and evaporated. The residue was triturated with diethyl ether, filtered and dried on a vacuum pump to afford title compound 138 as a yellow-brown solid (1.80 g, 79% yield). MS (m/z): 526.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093264B2
Source datasetuspto-grants-2012_01
ORD IDord-c51853fe18cb496ba0ad115dc16c341b
Source noteuspto-grants-2012_01