HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Toluenesulfonyl Isocyanate → Succinic anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Toluenesulfonyl Isocyanate | HCID 2733313 | — |
| Reactant | Di-n-butyldilauryltin | HCID 9809426 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Succinic anhydride | HCID 7922 | — |
| Product | Diethanolamine | HCID 8113 | — |
Reaction Steps
16.1 g of polypropylene glycol (M=480), 65.7 g of anhydrous tetrahydrofuran and 0.22 g of toluenesulfonyl isocyanate were stirred for 15 minutes in a three-necked flask with a capacity of 250 ml. 13 g of tolylene-2,4-diisocyanate and 0.17 g of dibutyltin dilaurate were then added and the mixture was heated under reflux for two hours. 6.9 g of the addition product formed from 1 mol of succinic anhydride and 1 mol of diethanolamine were then added and refluxing was continued for a further two hours. The solution was then diluted with 42.2 g of tetrahydrofuran and 1.95 g of polyoxypropylenediamine (M=420) in 42.2 g of tetrahydrofuran were added dropwise.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05053317 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-8316ee8fd5524f158a48a69ea30674ab |
| Source note | uspto-grants-1991_10 |