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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33698Generated: October 26, 2026

Acetic Acid → Ammonia methanol dichloromethane

https://huagongshe.com/reaction/33698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
Reactant1,1-DichloroethaneHCID 6365—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1-[4-(3-Pyrrolidin-1-yl-propoxy)-phenyl]-piperazine hydrochlorideHCID 9901844—
Product1-Benzyl-4-[4-(3-pyrrolidin-1-yl-propoxy)-phenyl]-piperazineHCID 9969991—
ProductAmmonia methanol dichloromethaneHCID 215841725%

Reaction Steps

A solution of the product of Example 23 (148 mg), benzaldehyde (520 mg), and acetic acid (25 mg) in dichloroethane (3 mL) was treated with sodium triacetoxyborohydride (121 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 light yellow solid (8 mg). 1H NMR (400 MHz, CDCl3): 7.36-7.24 (m, 5H), 6.94-6.81 (m, 4H), 3.96 (t, J=6.4 Hz, 2H), 3.56 (s, 2H), 3.08 (t, J=4.9 Hz, 4H), 2.64-2.60 (m, 4H), 2.04-1.94 (m, 2H), 1.80-1.75 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429586B2
Source datasetuspto-grants-2008_09
ORD IDord-accdf9f94e824b48ab1a2eac8bb2b6b7
Source noteuspto-grants-2008_09