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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259660Generated: October 31, 2026

Tetrahydrofuran → HCID 19707992, compound

https://huagongshe.com/reaction/259660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantHCID 54303134HCID 54303134—
CatalystPhenothiazineHCID 7108—
SolventChloroformHCID 6212—
ProductHCID 19707992HCID 1970799243%

Reaction Steps

A one liter, three necked flask was equipped with overhead stirrer, nitrogen atmosphere and an addition funnel. The flask was charged with 100 g of N,N'-di(hydroxyethyl)-N,N'-dimethyl phthalamide (0.36 mol.), 67.8 g of triethylamine (0.72 mol.), 500 ml of tetrahydrofuran and 2 g of phenothiazine. Next, 68 g of acryloyl chloride (0.75 mol.) was slowly added to the flask over one hour. The reaction was stirred for an additional hour. The triethylamine hydrochloride salt was removed by filtration and the remaining mother liquor was evaporated with a rotoevaporator to yield a light brown liquid. The liquid was dissolved in chloroform and washed with NaCl(aq.), NH4OH(10%), NaCl(aq.) and dried over MgSO4. The chloroform was removed with a rotoevaporator to yield 60 g (43%) of a light brown liquid. The product was confirmed by IR and 13C NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523152
Source datasetuspto-grants-1996_06
ORD IDord-134654f87cfb45379ed2c15d3cca4cdf
Source noteuspto-grants-1996_06