Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | L-Tryptophan, methyl ester | HCID 77980 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(Dimethylamino)-4-phenylcyclohexan-1-one | HCID 11424492 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 69337530 | HCID 69337530 | — |
Reaction Steps
The hydrochloride of L-tryptophan methyl ester (1.01 g) was stirred vigorously for 15 minutes with 1,2-dichloroethane (20 ml) and saturated NaHCO3 solution (20 ml) and the aqueous phase was immediately extracted with 1,2-dichloroethane (2×20 ml). After drying with Na2SO4, the organic phase was concentrated to 40 ml, and 4-dimethylamino-4-phenylcyclohexanone (893 mg, 4 mmol.) was added thereto under argon. Glacial acetic acid (0.228 ml, 4 mmol.) and Na2SO4 (2 g) were added to the clear solution. After a reaction time of 15 minutes, NaBH(OAc)3 (1.2 g) was added to the reaction mixture, and stirring was carried out for 4 days at room temperature. For working up, saturated NaHCO3 solution (40 ml) was added and stirring was carried out for 15 minutes. The aqueous phase was extracted with dichloromethane (2×20 ml). The combined organic phases were dried and then concentrated, yielding a light-brown oil. Purification by column chromatography was carried out with ethyl acetate and methanol. The nonpolar diastereomer (918 mg; m.p. 108-112° C.) was dissolved in 2-butanone (15 ml) and converted with chlorotrimethylsilane (0.4 ml) into the corresponding dihydrochloride (white solid; 326 mg; m.p. 197-202° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07276518B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-a9e8a77ef15e40a88a90419bc7c731b6 |
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| Source note | uspto-grants-2007_10 |
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