HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 70623967, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Octadecyl isocyanate | HCID 66988 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | HCID 15181656 | HCID 15181656 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 70623967 | HCID 70623967 | — |
Reaction Steps
A 5.7 g portion of the 10-amino-benzimidazo[2,1-a]benz[de]isoquinoline-7-one was added to 200 ml of distilled tetrahydrofuran in a 500 ml flask. To this mixture was added 5.9 g of Mondur O (octadecyl isocyanate) and 0.3 g of 1,4-diazobicyclo-octane. The mixture was stirred with a magnetic stirring bar and brought to reflux. The mixture was refluxed until no isocyanate peak was visible at 2240 cm-1 on infrared spectraphotometric analysis (~48-72 hours). It was then cooled and the solvent removed on the rotary evaporator. The solid thus obtained was ground to a fine powder, stirred in ether, filtered and dried in the vaccuum oven. The yield was 10.7 g of 10 octadecylureido benzimidazo [2,1-a]benz[de]isoquinoline-7-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04040968 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-5e31789563164e879c6fddc7ec5b4904 |
| Source note | uspto-grants-1977_08 |