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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33699Generated: October 26, 2026

Acetic Acid → Ammonia methanol dichloromethane

https://huagongshe.com/reaction/33699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetoneHCID 180—
Reactant1,1-DichloroethaneHCID 6365—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-[4-(3-Piperidin-1-yl-propoxy)-phenyl]-piperazine hydrochlorideHCID 9924012—
Product1-Isopropyl-4-[4-(3-piperidin-1-yl-propoxy)-phenyl]-piperazineHCID 9928168—
ProductAmmonia methanol dichloromethaneHCID 215841725%

Reaction Steps

A solution of the product of Example 25 (122 mg), acetone (23 mg), and acetic acid (19 mg) in dichloroethane (3 mL) was treated with sodium triacetoxyborohydride (96 mg). After 14 h, the reaction was quenched with saturated aqueous sodium bicarbonate, and the aqueous phase was extracted with dichloromethane (120 mL). The organic phase was dried (magnesium sulfate) and evaporated in vacuo. Silica gel chromatography of the residue (5% 2M ammonia-methanol/dichloromethane) gave the title compound as a white solid (31 mg). 1H NMR (400 MHz, CDCl3): 6.91-6.87 (m, 2H), 6.85-6.81 (m, 2H), 3.95 (t, J=6.4 Hz, 2H), 3.10 (t, J=4.9 Hz, 4H), 2.69 (t, J=4.9 Hz, 4H), 2.48-2.44 (m, 2H), 2.39 (bs, 4H), 1.98-1.91 (m, 2H), 1.61-1.56 (m, 4H), 1.46-1.40 (m, 2H), 1.09 (d, J=6.5 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429586B2
Source datasetuspto-grants-2008_09
ORD IDord-2eb1d2c5976f4473b28a36104e19f9c8
Source noteuspto-grants-2008_09