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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726813Generated: October 23, 2026

Phenothiazine → 5-Acryloyloxymethyl-oxazolidin-2-one

https://huagongshe.com/en/reaction/726813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenothiazineHCID 7108—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
Reactant5-(Hydroxymethyl)oxazolidin-2-oneHCID 10290773—
SolventTetrahydrofuranHCID 8028—
Product5-Acryloyloxymethyl-oxazolidin-2-oneHCID 18934230—

Reaction Steps

105 g (0.90 mol.) of 5-hydroxymethyl-oxazolidin-2-one were placed into a one liter, three necked, round bottomed flask equipped with a paddle stirrer and thermometer. This was followed by 500 ml of tetrahydrofuran, 101 g (1.0 mol.) of triethylamine and 0.5 g of phenothiazine. Stirring was started as 90 g (1.0 mol.) of acryloyl chloride were added dropwise in such a way that the contents of the flask were maintained at 30° C. or less. When the addition was complete, the contents were stirred overnight at room temperature. The triethylamine hydrochloride was filtered and the solution was allowed to stand over NaHCO3 and Na2SO4. The solution was filtered, transferred to a one liter, round bottomed flask and placed on a rotoevaporator. The solution was concentrated by purging with a stream of air while rotating the flask. The resulting liquid was confirmed by 13C NMR to contain a mixture of the desired product and unreacted starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05710281
Source datasetuspto-grants-1998_01
ORD IDord-b2be0e004c274725b6ab604156556335
Source noteuspto-grants-1998_01