HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379640Generated: October 25, 2026
1-(Chloromethyl)-4-(methylthio)benzene → 2-Methyl-3-(4-methylthiobenzyl)-1-indanone
https://huagongshe.com/reaction/379640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(Chloromethyl)-4-(methylthio)benzene | HCID 70128 | — |
| Reactant | 2-Methylindanone | HCID 249262 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-3-(4-methylthiobenzyl)-1-indanone | HCID 18367456 | — |
Reaction Steps
To a cooled solution (−70° C.) of LDA (1 M) in THF (37 mL) was added dropwise a solution of 2-methyl-1-indanone (J.A.C.S. Vol. 98, 8119-8124 (1976)) (2.5 g, 17 mmol) in THF (20 mL). The resulting dark red solution was stirred at room temperature for 3 hours, then cooled to −20° C. and a solution for 4-methylthiobenzyl chloride (3.1 g, 18 mmol) in THF (15 mL) was added slowly. The addition completed, the reaction mixture was stirred at −20° C. for 30 minutes before being quenched with 3N aqueous HCl (50 mL) and brine (50 mL). The product was extracted with ether, dried over MgSO4 and evaporated to dryness. The oily residue was chromatographed on silica gel eluting with a 1:5 mixture of ethyl acetate-hexane to afford the pure title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06300346B1 |
|---|
| Source dataset | uspto-grants-2001_10 |
|---|
| ORD ID | ord-6e463c8082fe4fbbbdd06b9eff4ef69d |
|---|
| Source note | uspto-grants-2001_10 |
|---|