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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971031Generated: November 2, 2026

Water → HCID 58096727, compound

https://huagongshe.com/reaction/1971031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
Reactant1,4-DioxaneHCID 31275—
ReactantAripiprazoleHCID 60795—
ProductHCID 58096727HCID 5809672770%

Reaction Steps

The chloromethyl ester above is dried over 4 Å molecular sieves. A solution of aripiprazole (45 grams, 0.1 mol) in 1,4-dioxane (800 mL) was sonicated to dissolve the aripiprazole completely, and then treated with NaH (38 g, 0.95 mol, 60% dispersion) in one portion. After stirring this reaction mixture for 15 minutes at room temperature, the reaction mixture was treated dropwise with chloromethyl ester (0.3 mol.) and a catalytic amount of sodium iodide (0.05 mol.). The resultant cloudy mixture was heated to 90° C. for 2 hours, cooled to ambient temperature and poured into water. The product was extracted with ethyl acetate, and the combined ethyl acetate layers washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Column chromatography over silica gel provided the desired product (12.5 gram, 70% yield). 1H NMR (CDCl3, 300 MHz) δ 0.87 (t, 3H), 1.20 (m, 12H), 1.63 (m, 2H), 1.70 (m, 2H), 1.83 (m, 2H), 2.35 (t, 2H), 2.50 (t, 2H), 2.68 (m, 6H), 2.86 (t, 2H), 3.08 (m, 4H), 3.97 (t, 2H), 5.92 (s, 2H), 6.58 (dd, 1H), 6.61 (d, 1H), 6.94 (dd, 1H), 7.06 (d, 1H), 7.14-7.17 (m, 2H); m/z (M+H) 632.88.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431576B2
Source datasetuspto-grants-2013_04
ORD IDord-45d46ea38dc548839e33f3d726b85eef
Source noteuspto-grants-2013_04