HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67586603, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 4,5,6,7-Tetrahydrofuro[2,3-c]pyridine hydrochloride | HCID 19599907 | — |
| Reactant | HCID 69554542 | HCID 69554542 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67586603 | HCID 67586603 | — |
Reaction Steps
To a solution of 1.173 g (7.349 mmol) of 4,5,6,7-tetrahydrofuro[2,3-c]pyridine hydrochloride, 1.90 g (7.35 mmol) of (Z)-4-chloro-4'-stilbenecarboxylic acid and 4.10 ml (29.4 mmol) of triethylamine in 30 ml of N,N-dimethylformamide, 1.34 ml (8.82 mmol) of diethyl cyanophosphonate was added dropwise, followed by overnight stirring at room temperature. This mixture was poured into water and extracted with diethyl ether 3 times. The combined organic layer was dried over anhydrous sodium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane/ethyl acetate=6/1 to 3/1) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05998433 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-5bd8be580f5e467b8791845758cb80dd |
| Source note | uspto-grants-1999_12 |