Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Eseroline | HCID 119198 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Phenserine | HCID 192706 | 96,456.5% |
Reaction Steps
Eseroline base (50 g, 0.229 mol) was dissolved in 400 mL anhydrous dimethoxyethane under an argon atmosphere. Catalytic amounts of 2.5 M n-butyl lithium in hexanes (6.4 mL, 16 mmol) were added within 1 minute and the solution stirred for 10 minutes. Phenyl isocyanate (27.269 g, 0.2286 mmol) was added over 32 minutes keeping the temperature between 20 and 23° C. The reaction solution was stirred at r.t. for 2 hours 20 minutes, then transferred to an addition funnel. The reaction solution was added over 49 minutes to mixture of DI water (630 mL) and dimethoxyethane (42 mL) under vigorous stirring. The obtained slurry was stirred for 30 minutes, then filtered via a Buchner funnel (Whatman #3 filterpaper). The solid residue was washed four times with DI water (100 mL each) and once with heptane (100 mL), then dried at 45° C. and >29 inches of vacuum for 9 hours. Phenserine base (74.4 g) was obtained as reddish solid in 96.2% yield and 95.1% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06495700B1 |
|---|
| Source dataset | uspto-grants-2002_12 |
|---|
| ORD ID | ord-72e00132dab244c2a805eae1fe56b228 |
|---|
| Source note | uspto-grants-2002_12 |
|---|