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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518227Generated: October 30, 2026

Phenylacetaldehyde → HCID 66932261, compound

https://huagongshe.com/reaction/518227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 66932407HCID 66932407—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 66932261HCID 6693226189.4%

Reaction Steps

(E)-3-{3,4-Dihydro-4-oxo-spiro[2H-(1,3)-benzoxazine-2,4′-piperidin]-6-yl}-acrylic acid methyl ester hydrochloride (obtained as described in Example 25, Step B, 300 mg, 0.886 mmol) was dissolved in MeOH (30 ml). The pH was adjusted to 5 with AcOH and 1 M NaOH in MeOH, and then phenyl-acetaldehyde (128 mg, 1.06 mmol) and NaCNBH3 (67 mg, 1.06 mmol) were added. The mixture was stirred overnight at RT, then the solvent was removed and the residue partitioned between 5% aqueous NaHCO3 and DCM. The organic phase was dried over Na2SO4 and evaporated. The crude product was purified by column chromatography (eluent: DCM/MeOH 95:5) to give (E)-3-{1′-(2-phenyl-ethyl)-3,4-dihydro-4-oxo-spiro[2H-(1,3)-benzoxazine-2,4′-piperidin]-6-yl}-acrylic acid methyl ester (322 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115148B2
Source datasetuspto-grants-2015_08
ORD IDord-9b8b7dd61b6144e4b62607aff9f7a981
Source noteuspto-grants-2015_08