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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45201Generated: October 25, 2026

Sodium Hydroxide → 1-(1,4-Dioxa-spiro[4.5]dec-8-yl)-1-phenyl-ethylamine

https://huagongshe.com/reaction/45201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,4-Dioxaspiro[4.5]decane-8-carbonitrileHCID 11116433—
ReactantHCID 178418255HCID 178418255—
ReactantHCID 178418348HCID 178418348—
CatalystTitanium isopropoxideHCID 11026—
SolventDiethyl EtherHCID 3283—
Product1-(1,4-Dioxa-spiro[4.5]dec-8-yl)-1-phenyl-ethylamineHCID 58381015—

Reaction Steps

Under argon, phenylmagnesium bromide (3M) in diethyl ether (6.7 mL, 20 mmol) was added to a solution of 1,4-dioxa-spiro[4.5]decane-8-carbonitrile (3.34 g, 20 mmol) in diethyl ether (60 mL). The mixture was stirred for 30 minutes. Titanium (IV) isopropoxide (5.7 g, 20 mmol) was then added. After stirring for 5 min, methyl lithium (1.6 M in diethyl ether, 31.2 mL, 50 mmol) was added and the reaction was heated under reflux for 10 hours. After cooling in ice/water the brown mixture was treated cautiously with 2M NaOH solution (30 mL) dropwise (exothermic). The mixture was extracted with t-butyl methyl ether and dried over sodium sulphate. After filtration the organic phase was evaporated to give 5 g of a pale yellow oil, which was used in the next step without further purification. Rt=2.10 min (Method 2). Detected mass: 261.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541449B2
Source datasetuspto-grants-2013_09
ORD IDord-7306a45cd4c24805a47794cf7597b8ed
Source noteuspto-grants-2013_09