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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991679Generated: October 31, 2026

Hydrochloric Acid → HCID 131723555, compound

https://huagongshe.com/reaction/991679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzene, (2-bromoethoxy)-HCID 68526—
ReactantTert-butyl 4-(2-hydroxyphenyl)piperazine-1-carboxylateHCID 11543684—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 131723555HCID 131723555—

Reaction Conditions

Temperature55 °C

Reaction Steps

The product from Step 1 above (0.55 g, 2.0 mmol) was added to a stirred solution of NaO-t-Bu (0.55 g, 2.0 mmol) in DME (5 mL). After 5 min, β-bromophenetole (0.56 g, 2.8 mmol) was added, and the reaction was stirred at 55° C. for 15 h. 2 M HCl was added, and the reaction mixture was stirred for another 3 h. The reaction mixture was concentrated in vacuo and the residue was partitioned between 2 M NaOH/CHCl3. The aqueous phase was extracted with CHCl3 (×3). The combined organic layers were dried (MgSO4), concentrated, and the residue was purified by chromatography on silica gel using CHCl3/MeOH/NH4OH (90:10:0.4) as eluent to give the free base of the title compound. The free base was treated with HCl/ether, and the resulting hydrochloride salt was dried (80° C., 1 mmHg) to afford 0.254 g (35%) of the title compound as a light brown semi-solid material that solidified upon standing. Anal. (C18H22N2O2.HCl. H2O) H, N; C: calc, 61.27; found, 61.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465467B1
Source datasetuspto-grants-2002_10
ORD IDord-a627dbbcc2d14820866e48da8b9d7301
Source noteuspto-grants-2002_10