HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → Dibenzyl 2-[(benzylsulfanyl)methyl]pentanedioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Dibenzyl 2-methylenepentanedioate | HCID 10947302 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Dibenzyl 2-[(benzylsulfanyl)methyl]pentanedioate | HCID 15410799 | 90.4% |
Reaction Steps
To a solution of dibenzyl 2-methylenepentanedioate (12.16 g, 37.5 mmol) in acetone (100 ml), was added benzylmercaptan (9.31 g, 75.0 mmol) and 4-dimethylaminopyridine (0.46 g, 3.75 mmol) with stirring. The reaction mixture was refluxed for 16 hours. The cooled solution was concentrated under reduced pressure and purified by column chromatography to yield 15.2 g (90%) of clear oil. 1H NMR (CDCl3): δ 2.0 (m, 2H), 2.3 (m, 2H), 2.5 (m, 1H), 2.6 (m 2H), 3.6 (s, 2H), 4.9 (s, 2H), 5.0 (m, 2H), 7.2-7.5 (m, 15H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05902817 |
| Source dataset | uspto-grants-1999_05 |
| ORD ID | ord-9b8dc6e65d324c39b7c51073f374266e |
| Source note | uspto-grants-1999_05 |