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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195708Generated: October 26, 2026

Formaldehyde → (S)-2-Benzyl-4-(3-cyclopentyloxy-4-methoxy-phenyl)-1-methylpiperazine

https://huagongshe.com/reaction/2195708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazineHCID 16725642—
SolventDichloromethaneHCID 6344—
Product(S)-2-Benzyl-4-(3-cyclopentyloxy-4-methoxy-phenyl)-1-methylpiperazineHCID 2362756891%

Reaction Steps

A solution of (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine (Example 2) (73 mg, 0.2 mmol) in CH2Cl2 (5 mL) was treated with a 37% aqueous formaldehyde solution (16.4 uL, 0.22 mmol) and stirred for 5 min after which time solid sodium triacetoxyborohydride (64 mg, 0.3 mmol) was added. The suspension was then stirred for 3 hr then quenched with a saturated aqueous NaHCO3 solution (2 mL). The organic component was separated, dried over MgSO4, filtered, and evaporated to an oil which was purified by silica gel flash chromatography with 5% MeOH/CH2Cl2 as eluant to afford product as a burgundy oil (69 mg, 91%). 1H NMR (CDCl3) 1.54-1.61 (m, 2H), 1.77-1.85 (m, 6H), 2.57 (s, 3H), 2.60-2.67 (m, 3H), 3.02-3.13 (m, 3H), 3.22-3.32 (m, 2H), 3.76 (s, 3H), 4.59-4.62 (m, 1H), 3.76 (s, 3H), 4.59-4.62 (M, 1H), 6.30 (dd, J=8.6, 2.9, 1H), 6.35 (d, J=8.6, 1H), 7.20-7.33 (m, 5H). 13C NMR 24.2 (CH2), 33.0 (CH2), 36.3 (CH2), 42.9 (CH3), 50.2 (CH2), 55.0 (CH2), 55.1 (CH2), 56.8 (CH3), 63.7 (CH), 80.4 (CH), 106.2 (CH), 107.8 (CH), 113.2 (CH), 126.4 (CH) 128.6, 129.5 (CH), 139.0 (CH), 144.5, 146.1, 148.4. LC/MS 5.10 min, [M+1]+ 381.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338405B2
Source datasetuspto-grants-2012_12
ORD IDord-bd14fffc88414dbbb95bc9ffcea38c52
Source noteuspto-grants-2012_12