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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179082Generated: October 30, 2026

1,2-Dichloroethane → HCID 69337767, compound

https://huagongshe.com/reaction/1179082

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAcetic AcidHCID 176—
ReactantSodium SulfateHCID 24436—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
ReactantHCID 46236462HCID 46236462—
ProductHCID 69337767HCID 69337767—

Reaction Steps

4-Dimethylamino-4-phenylcyclohexanone (877 mg), sodium sulfate (2 g) and glacial acetic acid (230 μl, 4 mmol.) were added under argon to rac-6-fluorotryptophan methyl ester (952 mg) in 1,2-dichloroethane (approx. 30 ml). After one hour's stirring at RT, sodium triacetoxyborohydride (1.33 g, 6 mmol.) was added and the mixture was stirred for two days at RT. For working up, the mixture was concentrated, the residue was taken up in ethyl acetate (30 ml) and 1M NaOH (25 ml), the clear phases were separated in a separating funnel, the aqueous phase was extracted three times with ethyl acetate (10 ml each time) and the combined extracts were dried and concentrated by evaporation. The residue obtained (1.72 g) was purified by flash chromatography (eluant: MeOH/EtOAc 1:2, then MeOH/EtOAc 1:1 and MeOH/NH3 400:1). A portion (261 mg) of the nonpolar diastereomer (868 mg) was dissolved in 2-butanone (7 ml), and the corresponding dihydrochloride was precipitated with chlorotrimethylsilane (227 μl) (white solid; 224 mg; m.p. 164-169° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276518B2
Source datasetuspto-grants-2007_10
ORD IDord-d684e573052c4670a1cfb8819a169e33
Source noteuspto-grants-2007_10