HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518227Generated: October 30, 2026
Phenylacetaldehyde → HCID 66932261, compound
https://huagongshe.com/reaction/518227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 66932407 | HCID 66932407 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66932261 | HCID 66932261 | 89.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115148B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-9b8b7dd61b6144e4b62607aff9f7a981 |
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| Source note | uspto-grants-2015_08 |
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