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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808130Generated: November 1, 2026

Acetic Acid → HCID 68785177, compound

https://huagongshe.com/reaction/1808130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium SulfateHCID 24436—
Reactant95373-47-0HCID 178777—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
Solvent1,2-DichloroethaneHCID 11—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68785177HCID 68785177—

Reaction Steps

D,L-tryptophanamide hydrochloride (1.49 g, 6.25 mmol) was vigorously stirred with 1,2-dichloroethane (30 ml), tetrahydrofuran (20 ml) and saturated NaHCO3 solution (40 ml) for 15 min and the aqueous phase was then immediately extracted with a tetrahydrofuran/ethyl acetate mixture (1:3.5×40 ml). After drying with Na2SO4 the organic phase was concentrated to low volume. The released base (1.03 g, 5.06 mmol) and 4-(dimethylamino)-4-phenylcyclohexanone (1.09 g, 5.06 mmol) were dissolved in tetrahydrofuran (40 ml) and 1,2-dichloroethane (30 ml) in argon. Glacial acetic acid (0.291 ml, 5.06 mmol) and Na2SO4 (2.53 g) were added to the clear solution. After a reaction time of 15 min the reaction mixture was mixed with NaBH(OAc)3 (1.52 g, 7.08 mmol) and stirred for 2 d at room temperature. For work up of the batch the mixture was mixed with saturated NaHCO3 solution (60 ml) and stirred for 15 min. The aqueous phase was extracted with dichloromethane (2×40 ml). The combined organic phases were concentrated to low volume after drying, and a light brown oil was obtained. The chromatographic separation of the substance mixture on silica gel 60 (150 g) was conducted with ethyl acetate/methanol (1:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357705B2
Source datasetuspto-grants-2013_01
ORD IDord-af49b71708b443a1850828329510adf6
Source noteuspto-grants-2013_01