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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771013Generated: October 30, 2026

Hydrochloric Acid → Tapentadol Hydrochloride

https://huagongshe.com/reaction/1771013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant3(3-Methoxyphenyl)-N,N,2-trimethyl pentane-1-amine, (2R,3R)-HCID 11253328—
SolventDichloromethaneHCID 6344—
ProductTapentadol HydrochlorideHCID 983802190%

Reaction Steps

The product of Example 16 (1.9 g, 8 mmol) was dissolved in dichloromethane, the mixture was cooled in an ice-water bath, and a solution of boron tribromide (1.9 ml, 20 mmol) in dichloromethane was slowly added dropwise, then it was gradually raised to room temperature to make it react for 15 hrs. After it was cooled in an ice-water bath, methanol was slowly added dropwise to quench the reaction, and the organic phase was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated to 2 mL, then the concentrated hydrochloric acid (670 Ml, 8 mmol) was added dropwise, and the mixture was concentrated and recrystallized with isopropanol and ethyl acetate to obtain the target 1.8 g, yield: 90%. [α]D=+24.3° (c=1.10, CH3OH). 1HNMR (300 MHz, CD3OD): δ 7.2 (1H, t, J=7.9, 15.6), 6.6-6.8 (3H, m), 2.8-2.9 (2H, m), 2.7-2.8 (6H, br s), 2.2-2.3 (1H, m), 2.1-2.2 (1H, m), 1.8-1.9 (1H, m), 1.5-1.6 (1H, m), 1.2 (3H, d, J=6.7), 0.8 (3H, t, J=7.4, 14.4). ESI-MS: 222.4 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249084B2
Source datasetuspto-grants-2016_02
ORD IDord-fc5cc3de51754e2ba9eb9daa14d8b7f4
Source noteuspto-grants-2016_02