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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441930Generated: November 1, 2026

HCID 46929757, compound → HCID 11637664, compound

https://huagongshe.com/reaction/1441930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 46929757HCID 46929757—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 11637664HCID 11637664—

Reaction Steps

A mixture of hexyl-carbamic acid 1-benzyl-1, 2, 3, 4-tetrahydro-quinolin-6-yl ester (0.732 g., 2 mmol) and 5% Pd—C (0.08 g.) in absolute ethanol (20 ml) was shaken in a par apparatus at room temperature (38° C.) under 50 psi pressure of hydrogen for 4 hours. Pd—C was then discarded through filtration. The reaction mixture was concentrated under vaccum and the separated solid was washed with chloroform (2×5 ml) to give 2a; yield: 0.60 g. (64.1%), m.p.: 100° C., C16H24N2O2; 1H NMR δ ppm (CDCl3): 0.88 (bs, 3H), 1.25-1.30 (m, 5H), 1.51-1.58 (m, 3H), 1.85-1.97 (m, 3H), 2.74 (t, 2H), 3.16-3.29 (m, 4H), 3.6 (bs, 1H), 4.87 (bs, 1H), 6.39-6.4 (m, 1H), 6.68-6.71 (m, 2H), IR vmax (KBr) (cm−1): 770, 816, 886, 956, 1006, 1101, 1152, 1221, 1243, 1311, 1354, 1505, 1626, 1702, 1848, 2372, 2856, 2929, 3392, 3760, 3809, 7874, MS: m/z: 277 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655801B2
Source datasetuspto-grants-2010_02
ORD IDord-e2dc10dce34045fc9d767be2becf1740
Source noteuspto-grants-2010_02