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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344880Generated: October 29, 2026

Hydrogen Bromide → HCID 1514413, compound

https://huagongshe.com/reaction/344880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantPhenolHCID 996—
ReactantDiisopropyl EtherHCID 7914—
ReactantHCID 53899556HCID 53899556—
SolventWaterHCID 962—
ProductHCID 1514413HCID 151441366.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of (R)-2-phenyl-1,4-bis(p-toluenesulphonyl)piperazine (10 g) and phenol (9.4 g) in 48% strength hydrobromic acid (100 cc) is heated with very vigorous stirring to a temperature in the region of 120° C. for 5 hours. After cooling to approximately 80° C., the reaction mixture is treated with water (250 cc), cooled to about 20° C. and washed with dichloromethane (5×100 cc). The aqueous phase is concentrated under reduced pressure (20 kPa) at approximately 80° C. The residue is taken up with ethyl acetate (100 cc), cooled to 5° C. and treated at between 5° and 20° C. with 30% strength aqueous sodium hydroxide (100 cc). The organic phase is separated and the aqueous phase extracted again with ethyl acetate (3×100 cc). The combined organic extracts are washed with 5N aqueous sodium hydroxide (4×20 cc), dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (20 kPa) at approximately 30° C. The residue obtained is taken up with isopropyl ether (15 cc) at approximately 0° C., drained and washed at the same temperature with the same solvent (10 cc). (R)-2-Phenylpiperazine (2.3 g) is obtained in the form of a colorless solid, m.p. 117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05053509
Source datasetuspto-grants-1991_10
ORD IDord-7ddc53ea8f634a7caba2c2f6618aa0e4
Source noteuspto-grants-1991_10