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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519702Generated: November 2, 2026

Sodium Bicarbonate → HCID 86679269, compound

https://huagongshe.com/reaction/1519702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-EthynylbenzaldehydeHCID 2771645—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant1,4-Oxazepane hydrochlorideHCID 23090214—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
ProductHCID 86679269HCID 8667926989.5%

Reaction Steps

1,4-Oxazepane hydrochloride (1.0 g) and TEA (1.1 mL) were added to a chloroform (20 mL) solution of 4-ethynylbenzaldehyde (1.0 g) obtained by the same method as the synthesis method described in the literature (Tetrahedron Letters, 2007, Vol. 48(33), pp. 5817-5820). The mixture was stirred for 30 minutes at room temperature, and acetic acid (0.45 mL) was added, followed by stirring the mixture for 1 hour at room temperature. Then, sodium triacetoxyborohydride (2.4 g) was added, and the mixture was stirred for 15 hours at room temperature. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and then the mixture was extracted with chloroform. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. Then, the desiccant was filtered out, and the solvent was distilled off under reduced pressure. The resulting residue was purified by NH type silica gel chromatography (gradient elution with hexane/ethyl acetate=90/10→60/40) to obtain 4-(4-ethynylbenzyl)-1,4-oxazepane (yellow solid) (1.4 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073821B2
Source datasetuspto-grants-2015_07
ORD IDord-5ac7ebb3b6594191892e20445842458e
Source noteuspto-grants-2015_07