HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-Chloro-1-hydroxymethyl-8-methylcarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 7-Chloro-8-methylcarbazole-1-carboxylic acid | HCID 21399931 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Chloro-1-hydroxymethyl-8-methylcarbazole | HCID 21399934 | 95% |
Reaction Steps
A suspension of 0.3 g. of lithium aluminum hydride in 5 ml. of absolute tetrahydrofuran is combined dropwise with 0.560 g. of the ethyl ester of 7-chloro-8-methylcarbazole-1-carboxylic acid, dissolved in 10 ml. of absolute tetrahydrofuran; the mixture is agitated for one hour at room temperature. Then, the reaction mixture is heated for one hour under reflux, allowed to cool, diluted with 20 ml. of ethyl acetate, mixed under cooling dropwise with hydrochloric acid, and the organic phase is separated, washed, and concentrated under vacuum. The residue is recrystallized from toluene, thus obtaining, in a 95% yield, 7-chloro-1-hydroxymethyl-8-methylcarbazole, m.p. 187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03956295 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-85c2c1a5010546d0b0e8ffda6fb8abcb |
| Source note | uspto-grants-1976_05 |