HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 69510007, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 18465958 | HCID 18465958 | — |
| Reactant | HCID 69512330 | HCID 69512330 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69510007 | HCID 69510007 | 61% |
Reaction Steps
3.3 g of 4-(6-acryloyloxyhexyloxy)benzoyl chloride dissolved in 40 ml of dichloromethane was added dropwise to a solution of 2.4 ml of triethylamine, 0.3 g of 4-N,N′-dimethylaminopyridine and 1.8 g of 3-(R)-hydroxy-hexahydro-furo[3,2-b]furan-6-(S)-yl 4-hydroxycinnamate (26) in 40 ml of dichloromethane. The reaction was stirred overnight at room temperature. The solution was extracted with 80 ml of 2.5 N HCl. The organic layer was washed with water, dried over MgSO4 and passed through a silica pad. The solvent was evaporated. The crude producty was recrystallised twice from ethyl acetate. 2.8 g of white crystals were obtained (yield: 61%). The melting point of the compound was 142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07311948B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-a48b1c9fba624640a6b0eb74c3bf8fb4 |
| Source note | uspto-grants-2007_12 |