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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255305Generated: November 2, 2026

tert-Butyl acrylate → tert-Butyl 3-(4-(2-(4-(2-ethylthiazole-4-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)ethyl)phenethoxy)propanoate

https://huagongshe.com/reaction/1255305

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant(2-Ethylthiazol-4-yl)(9-(4-(2-hydroxyethyl)phenethyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanoneHCID 58168519—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 3-(4-(2-(4-(2-ethylthiazole-4-carbonyl)-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)ethyl)phenethoxy)propanoateHCID 58168598—

Reaction Steps

N,N,N-Trimethyl-1-phenylmethanaminium hydroxide (40% in water, 0.51 mL) was added to a solution of (2-ethylthiazol-4-yl)(9-(4-(2-hydroxyethyl)phenethyl)-1-oxa-4,9-diazaspiro[5.5]undecan-4-yl)methanone [Example 3, step c] (1.9 g) and tert-butyl acrylate (1.32 mL) in acetonitrile (1.5 mL) and the mixture stirred at ambient temperature for 4 hours. The mixture was concentrated in vacuo and the crude product purified by flash silica chromatography, elution gradient 50 to 75% ethyl acetate in isohexane with 5% triethylamine. Fractions containing the product were evaporated to dryness to afford the subtitled compound as a colourless oil. Yield 2.19 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455483B2
Source datasetuspto-grants-2013_06
ORD IDord-994897e158504137a8abba9f621841dc
Source noteuspto-grants-2013_06