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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704611Generated: October 31, 2026

Ammonium Chloride → HCID 15735660, compound

https://huagongshe.com/reaction/704611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantChloromethyl pivalateHCID 87885—
ReactantHCID 15735587HCID 15735587—
SolventDimethylformamideHCID 6228—
SolventDCM MeOH AcOHHCID 21877243—
ProductHCID 15735660HCID 1573566064.4%

Reaction Steps

To a solution of 100 mg (0.347 millimole) of (Z)-3-cyclohexyl-2-(hydroxyisobutylphosphinoyl)methylpropenoic acid in 1.0 ml of dimethylformamide were added 130 μl (0.87 millimole) of 1,8-diazabicyclo[5,4,0]-7-undecene and 75 μl (0.52 millimole) of chloromethyl pivalate, and the mixture was stirred at room temperature for 21 hours. Fifty milliliters of a saturated aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted three times with 30 ml of ethyl acetate each time. The combined organic layers were washed with 10 ml of a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by preparative thin-layer chromatography silica gel 60 F254 made by E. Merck & Co.; dichloromethane/methanol/acetic acid [30:1:1)] to give 90 mg (yield 64%) of the captioned compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988681
Source datasetuspto-grants-1991_01
ORD IDord-8556b961c32b43c797607a00d6d7b13e
Source noteuspto-grants-1991_01