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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908032Generated: October 31, 2026

Hydroxylamine → tert-Butyl (4E)-4-(hydroxyimino)-3,4-dihydro-1'H-spiro[1-benzopyran-2,4'-piperidine]-1'-carboxylate

https://huagongshe.com/reaction/1908032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantWaterHCID 962—
ReactantTert-butyl 4-oxo-3,4-dihydrospiro[1-benzopyran-2,4'-piperidine]-1'-carboxylateHCID 40427565—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl (4E)-4-(hydroxyimino)-3,4-dihydro-1'H-spiro[1-benzopyran-2,4'-piperidine]-1'-carboxylateHCID 5855161998%

Reaction Steps

tert-Butyl 4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate (450 mg, 1.41 mmol) and hydroxylamine 50 wt % in water (940 μL, of 50% w/v, 14 mmol) were combined in methanol (9.0 mL) and heated at reflux. After 24 hours, the reaction mixture was diluted with ethyl acetate and was washed with water. The organics were dried over MgSO4, filtered and evaporated to dryness to yield (E)-tert-butyl 4-(hydroxyimino)spiro[chroman-2,4′-piperidine]-1′-carboxylate (450 mg, 98%). ESI-MS m/z calc. 332.4. found 333.3 (M+1)+; Retention time: 1.68 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598164B2
Source datasetuspto-grants-2013_12
ORD IDord-c6f6e1707d5943b782bbb5f85e123c80
Source noteuspto-grants-2013_12