HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-benzoyl-5-chloromethyl-2,3-dihydro-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 1-benzoyl-2,3-dihydro-1H-indole | HCID 681214 | — |
| Reactant | Carbon tetrachloride hexane | HCID 21584008 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-benzoyl-5-chloromethyl-2,3-dihydro-1H-indole | HCID 13021428 | 60% |
Reaction Steps
1-Benzoyl-2,3-dihydro-1H-indole (Beilstein, 20, 257) (5.58 g, 25 mmole) is dissolved in 50 ml of glacial acetic acid, then 56 ml (ca 70 mmoles) of 40% formaldehyde are added, and dry hydrogen chloride passed into the solution which is maintained at 70° for 3 hours. The solution is evaporated, and the residue dissolved in benzene, and again evaporated to dryness to give 6.53 g of crude product. This residue is treated with carbon tetrachloride-hexane to give 4.05 g (60%) of 1-benzoyl-5-chloromethyl-2,3-dihydro-1H-indole, m.p. 107.5 - 110.0°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04065572 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-0118f3f8e93249538dcee4c5031e870d |
| Source note | uspto-grants-1977_12 |