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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167513Generated: October 29, 2026

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

https://huagongshe.com/reaction/2167513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
Reactant3-MethoxybenzaldehydeHCID 11569—
Reactant1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
Product8-(3-Methoxybenzyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 647038782.8%

Reaction Steps

A mixture of 3-methoxybenzaldehyde (10.0 g, 73.4 mmol), 1,4-dioxa-8-azaspiro[4.5]decane (21.0 g, 146.9 mmol), sodium triacetoxyborohydride (31.1 g, 146.9 mmol), and acetic acid (4.4 mL, 73.45 mmol) in 1,2-dichloroethane (100 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 (200 mL). The combined organic layers were washed with brine (100 mL), dried over anhydrous sodium sulfate and concentrated in vacuo to provide 8-(3-methoxybenzyl)-1,4-dioxa-8-azaspiro[4.5]decane (16.0 g, 82%) as a yellow oil: 1H NMR (CDCl3, 400 MHz) δ 7.27-7.20 (m, 1H), 6.93-6.88 (m, 2H), 6.79 (dd, J=2.4, 8.2 Hz, 1H), 3.94 (s, 4H), 3.82-3.78 (m, 3H), 3.50 (s, 2H), 2.56-2.47 (m, 4H), 1.74 (t, J=5.6 Hz, 4H); ESI MS (m/z) 264 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045468B2
Source datasetuspto-grants-2015_06
ORD IDord-67e75fa270eb48eabeb5070e4db10e69
Source noteuspto-grants-2015_06