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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51205Generated: October 25, 2026

Potassium Carbonate → 2-[4-(2,3-Dihydro-benzo[1,4]dioxin-5-yl)-piperazin-1-yl]-propan-1-ol

https://huagongshe.com/reaction/51205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(R)-(-)-2-Amino-1-propanolHCID 80308—
ReactantLithium BromideHCID 82050—
ReactantMethanesulfonic Acid 2-[(2,3-dihydro-benzo[1,4]dioxin-5-yl)-(2-methanesulfonyloxy-ethyl)-amino]-ethyl esterHCID 11383877—
SolventAcetonitrileHCID 6342—
Product2-[4-(2,3-Dihydro-benzo[1,4]dioxin-5-yl)-piperazin-1-yl]-propan-1-olHCID 10171603—

Reaction Conditions

Temperature82 °C

Reaction Steps

Dimesylate III (67.0 g, 0.17 mol), D-alaninol (14.0 g, 0.19 mol), lithium bromide (31.0 g, 0.35 mol), and potassium carbonate (74.8 g, 0.54 mol) are mixed together with acetonitrile (750 mL). The resulting suspension is refluxed (82° C.) for 27 h with monitoring by HPLC. The reaction mixture is cooled, filtered, and insoluble residue washed with acetonitrile. Mother liquor is concentrated to a small volume, filtered through 200 cm3 of silica gel, and eluted with 1.5 L of MeOH 10% in EtOAc. After removing solvent on rotary evaporator, the residue is redissolved in EtOAc (200 mL). This solution is washed with water (2×50 mL), dried with MgSO4 and concentrated to produce IV as thick golden oil that slowly crystallizes upon standing; yield 29.4 g (63%) and purity 88.3 area % (LC-MS). Melting point=91-92° C. 1H NMR (CDCl3) δ6.78 (t, J=7.5 Hz, 1H), 6.55 (m, 2H), 4.29 (m, 4H), 3.45 (dd, J=11, 5 Hz, 1H), 3.38 (t, J=11 Hz, 1H), 3.10 (br m, 4H), 2.86 (m, 3H), 2.63 (m, 2H), 0.96 (d, J=7.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713626B2
Source datasetuspto-grants-2004_03
ORD IDord-cbc164384c784410b134c01dbf34ef39
Source noteuspto-grants-2004_03