Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479814Generated: November 1, 2026

Phenylacetaldehyde → HCID 21904393, compound

https://huagongshe.com/reaction/479814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
ReactantHCID 69593428HCID 69593428—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 21904393HCID 2190439392%

Reaction Steps

Phenylacetaldehyde (0.87 mL, 7.40 mmol) was added to a solution of (8-benzyloxycarbonyl-1,4-dioxa-8-aza-spiro[4.5]-decane-6-ylmethyl)-N-phenylpropionamide (96) in MeOH (49.4 mL, 0.03M) in a hydrogenation flask. 20% Pd/C (0.53 g) was added, and the mixture was shaken under 40 psi H2 until the consumption of H2 ceased and the reaction was judged complete by TLC (3.5 h). The crude reaction mixture was passed through a column of Celite, concentrated in vacuo, arid purified by flash column chromatography (60:38:2::Hexanes:CH2Cl2:2N NH3 in EtOH) to obtain pure (8-phenethyl-1,4-dioxa-8-aza-spiro[4. 5]-decane-6-ylmethyl)-N-phenylpropionamide (97) (0.59 g, 92%). 1H NMR (CDCl3): 7.42-7.12 (10H, m), 4.08 (1H, dd, J=13.4, 9.5 Hz), 3.96-3.77 (4H, m), 3.65 (1H, broad d, J=10.9 Hz), 2.92-2.80 (1H, m), 2.80-2.64 (3H, m), 2.64-2.51 (2H, m), 2.33 (2H, broad t, J=10.3 Hz) 2.20-1.94 (3H, m), 1.72 (1H, dt, J=13.3, 13.2, 3.7 Hz), 1.58 (1H, ddd, J=13.1, 10.9, 4.3 Hz), 1.03 (3H, t, J=7.4 Hz) ppm. LRMS: 408.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645980B1
Source datasetuspto-grants-2003_11
ORD IDord-7ce0a3f749354b549d8e8b8a315b228b
Source noteuspto-grants-2003_11