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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385779Generated: October 29, 2026

Diisopropylamine → 8-(Phenylmethyl)-3-oxa-1,8-diazaspiro[4.5]decan-2-one

https://huagongshe.com/reaction/385779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium HydroxideHCID 14923—
ReactantTriphosgeneHCID 94429—
ReactantHCID 22020939HCID 22020939—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product8-(Phenylmethyl)-3-oxa-1,8-diazaspiro[4.5]decan-2-oneHCID 57780943—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 1 L 4-neck round bottom flask was added (4-amino-1-benzylpiperidin-4-yl)methanol (21.86 g, 99 mmol) and diisopropyl amine (23.0 g, 249 mmol) in dry toluene (300 ml). The reaction mixture was cooled to 0° C. and a solution of triphosgene (35.57 g, 119 mmol) in toluene (100 ml) was added. The reaction mixture was heated to 60° C. for 1.5 h. After cooling to room temperature, the reaction mixture was diluted with water (200 ml), basified with aqueous NH4OH, and extracted with ethyl acetate (3×200 ml). The organic layers were combined and washed with two 200 ml portions of water and 200 ml of brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The solid was stirred in hexanes for 1.5 hours and filtered again to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-320ca4f908cc474bae0d74b4ba3de81e
Source noteuspto-grants-2013_02