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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545213Generated: October 29, 2026

Sodium Bicarbonate → 1'-(tert-Butoxycarbonyl)-4-oxo-3,4-dihydrospiro[1-benzopyran-2,4'-piperidine]-6-carboxylic acid

https://huagongshe.com/reaction/545213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66782663HCID 66782663—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
Product1'-(tert-Butoxycarbonyl)-4-oxo-3,4-dihydrospiro[1-benzopyran-2,4'-piperidine]-6-carboxylic acidHCID 50999192—

Reaction Steps

6-Carboxy-4-oxospiro(chroman-2,4′-piperidine) hydrochloride (15.0 g, 50.3 mmol) was dissolved in 1,4-dioxane (150 ml) and H2O (150 ml), NaHCO3 (10.6 g, 126 mmol) and DIBOC (13.2 g, 60.4 mmol) were added thereto in this order. After stirred at room temperature for 13 h, the reaction mixture was diluted with Et2O and 5N NaOH aq. (12.1 ml). The aqueous layer was washed with Et2O and acidified with 6N HCl aq. (PH=ca. 3), then extracted with CHCl3. The organic layer was washed with brine and dried over MgSO4. The desiccant was removed through filtration and the filtrate was concentrated under reduced pressure. The residue was triturated with MeOH—H2O and the insoluble solid was collected through filtration to obtain the intended compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935712B2
Source datasetuspto-grants-2011_05
ORD IDord-e5924a9af78a436e9611a942597a3692
Source noteuspto-grants-2011_05