HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726482Generated: October 29, 2026
Tetrahydrofuran → HCID 19707992, compound
https://huagongshe.com/reaction/726482
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 54303134 | HCID 54303134 | — |
| Catalyst | Phenothiazine | HCID 7108 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 19707992 | HCID 19707992 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05709935 |
|---|
| Source dataset | uspto-grants-1998_01 |
|---|
| ORD ID | ord-fc8a57c514484b1c8f9004bd47e5d28b |
|---|
| Source note | uspto-grants-1998_01 |
|---|