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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094920Generated: October 26, 2026

Water → Tapentadol

https://huagongshe.com/reaction/1094920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantL-MethionineHCID 6137—
ReactantMethanesulfonic AcidHCID 6395—
Reactant3(3-Methoxyphenyl)-N,N,2-trimethyl pentane-1-amine, (2R,3R)-HCID 11253328—
SolventMethylcyclohexaneHCID 7962—
ProductTapentadolHCID 983802289.5%

Reaction Conditions

Temperature82 °C

Reaction Steps

18.9 kg of methanesulfonic acid and 2458 g D,L methionine were placed in methyl cyclohexane and then 3192 g (2R,3R)-[3-(3-methoxy-phenyl)-2-methyl-pentyl]-dimethylamine were added and the mixture was stirred at 82° C. for 18 hours. Subsequently, dilution was carried out with 10.3 l water at a maximum of 80° C. and 9 l methyl cyclohexane were added. At a maximum of 42° C., 17.3 l ammoniac were added until the pH was 8.8. A phase separation took place at 45° C. and 3.2 g (1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol were added to the organic phase at 40° C. and stirred for 1 hour at 36° C. Subsequently, after cooling slowly to 5° C. and a further hour of stirring, the precipitate which formed was extracted by suction, washed with 12 l methyl cyclohexane and dried in a drying chamber. 2685 g (89.5%) (1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol were obtained in modification B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134032B2
Source datasetuspto-grants-2012_03
ORD IDord-3a1c836cbeee4b5a93f69b14b95b1075
Source noteuspto-grants-2012_03