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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167507Generated: November 3, 2026

Sodium Carbonate → 8-(3-Methoxybenzyl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/2167507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-MethoxybenzaldehydeHCID 11569—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product8-(3-Methoxybenzyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 647038795%

Reaction Steps

A mixture of 3-methoxybenzaldehyde (10.0 g, 73.4 mmol), 1,4-dioxa-8-azaspiro[4.5]decane (10.5 g, 73.4 mmol), sodium triacetoxyborohydride (20.2 g, 95.3 mmol), and acetic acid (4.2 mL), in methylene chloride (400 mL), was stirred at ambient temperature. After 19 h, a 2 N aqueous sodium carbonate solution (220 mL) was added portionwise. After stirring for 15 min, the aqueous layer was separated and extracted with methylene chloride (100 mL). The combined organic layers were washed with brine (100 mL), dried over sodium sulfate and concentrated in vacuo to provide 8-(3-methoxybenzyl)-1,4-dioxa-8-azaspiro[4.5]decane (18.3 g, 95%) as a yellow oil: 1H NMR (CDCl3, 500 MHz) δ 7.25-7.19 (m, 1H), 6.91-6.89 (m, 2H), 6.80-6.77 (m, 1H), 3.94 (s, 4H), 3.80 (s, 3H), 3.50 (s, 2H), 2.53-2.49 (m, 4H), 1.76-1.72 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045468B2
Source datasetuspto-grants-2015_06
ORD IDord-7788a472b76a445d977d36ce639e3145
Source noteuspto-grants-2015_06