HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → 2-(6-Benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 2-(6-Bromohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde | HCID 19930264 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(6-Benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde | HCID 19930289 | — |
Reaction Steps
A solution of sodium ethoxide (69 mg sodium, 3 mmol in ethanol 1 ml) was added to a stirred suspension of 2-(6-bromohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde (0.98 g, 3 mmol) and benzyl mercaptan (0.35 g, 3 mmol) in ethanol (10 ml) at room temperature under nitrogen. After 1 hour evaporated, water (10 ml) and 2M sodium hydroxide (2 ml) added and extracted with diethyl ether (10 ml). The extracts were washed with water, dried, filtered and evaporated to an oil (1.12 g). Chromatography on silica eluting with dichloromethane gave 2-(6-benzylthiohexyloxy)-5-methyl-1,3-benzenedicarboxaldehyde as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428065 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-7f6483fff6624318bcdbcd4153c44add |
| Source note | uspto-grants-1995_06 |