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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507285Generated: October 29, 2026

3,4-Dihydro-1'-(phenylmethyl)spiro[naphthalene-1(2H),4'-piperidine] → HCID 15637617, compound

https://huagongshe.com/reaction/507285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dihydro-1'-(phenylmethyl)spiro[naphthalene-1(2H),4'-piperidine]HCID 125328—
ReactantAmmonium formateHCID 2723923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 15637617HCID 15637617—

Reaction Steps

A suspension of 1′-benzyl-3,4-dihydro-2H-spiro[naphthalene-1,4′-piperidine] 17a (1.7 g, 5.8 mmol), 10% Pd/C (1 g), and ammonium formate (4.8 g, 76 mmol) in MeOH (50 ml) was stirred under N2 for 24 hours. The mixture was filtered through Celite, and the filtrate was concentrated. The filtrate was dissolved in CH2Cl2, washed with diluted NaOH, and the aqueous phase was re-extracted with CH2Cl2. The combined organic phase was dried (Na2SO4) and concentrated to give 3,4-dihydro-2H-spiro[naphthalene-1,4′-piperidine] 17b. LC-MS: m/e=202.1 (M+H). Rt=1.61 min. 1H-NMR (500 MHz, CDCl3): 9.74 (s, 2H), 7.58 (d, J=7.9, 1H), 7.22 (t, J=7.8, 1H), 7.14 (t, J=7.9, 1H), 7.08 (d, J=8.0, 1H), 3.47 (d, J=12.4, 2H), 3.22-3.18 (m, 2H), 2.88 (t, J=4.9, 2H), 2.81 (t, J=6.2, H), 2.60 (td, 2H), 1.93-1.89 (m, 2H), 1.83-1.77 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786141B2
Source datasetuspto-grants-2010_08
ORD IDord-ad2a7762c99f4bd6aa3b5df3f33c15ac
Source noteuspto-grants-2010_08