HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-chloropropane → 6-Chloro-3-(3-chloropropyl)-2(3H)-benzothiazolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 53400706 | HCID 53400706 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-Chloro-3-(3-chloropropyl)-2(3H)-benzothiazolone | HCID 19003508 | 93.5% |
Reaction Steps
A solution of 6-chloro-benzothiazolone (VIII) (55.7 g, 0.3 mol), K2CO3 (62.1 g, 0.45 mol) and 1-bromo-3-chloropropane (IX) (71 g, 0.45 mol) in acetone (600 ml) was refluxed for 16 hours. After cooling, the inorganic substance was filtered off and washed dichloromethane. The filtrate and washings were combined and evaporated in vacuo. The residue was washed with hexane and recrystallized from dichloromethane to obtain compound (X) (73.5 g, yield=93.4%) as colorless needle-shaped crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05473066 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-fc6c6655846d4acfaf8a67555ceb05d1 |
| Source note | uspto-grants-1995_12 |