HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → alpha-(5-Chloropentyl)-3,4-dimethoxy-alpha-[(4-methylphenyl)-thio]benzeneacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-5-chloropentane | HCID 96070 | — |
| Reactant | 3,4-Dimethoxy-alpha[(4-methylphenyl)thio]benzeneacetonitrile | HCID 10542167 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | alpha-(5-Chloropentyl)-3,4-dimethoxy-alpha-[(4-methylphenyl)-thio]benzeneacetonitrile | HCID 10573255 | 90% |
Reaction Steps
To a stirred solution of 5.00 g of 3,4-dimethoxy-α-[(4-methylphenyl)thio]benzeneacetonitrile in 50 mL of N,N-dimethylformamide, under an argon atmosphere, is added 0.73 g of 60% sodium hydride in oil. After 1.5 hours, 4.65 g of 1-bromo-5-chloropentane is added to the resulting solution and stirring continued for 3 hours. The reaction is poured into ice water, and twice extracted with diethyl ether. The combined organic extracts are dried (magnesium sulfate), and concentrated in vacuo to give a golden oil. Purification by chromatography on a silica gel column using diethyl ether/hexane (2:3), affords 6.07 g of the desired product as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05387685 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-d26bf99d644c4db8aa1181f04dc9144f |
| Source note | uspto-grants-1995_02 |