HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aluminium lithium hydride → (+/-) trans 1-(3,4-Dichlorophenylthio)-2-methylaminoindane Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | (+/-) trans 1-(3,4-Dichlorophenylthio)-2-ethoxycarbonylaminoindane | HCID 53664910 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (+/-) trans 1-(3,4-Dichlorophenylthio)-2-methylaminoindane Hydrochloride | HCID 86752857 | — |
Reaction Steps
To a suspension of LiAlH4 (0.34 g, 9.05 mmol) in dry diethyl ether under nitrogen was added a solution of (±) trans 1-(3,4-dichlorophenylthio)-2-ethoxycarbonylaminoindane (0.69 g, 1.81 mmol) in diethyl ether. After stirring at room temperature overnight, the reaction was worked up as described for Example 2, and then purified on a silica gel column using 1% ethanol in chloroform as eluant. The resulting oil (0.26 g) was extracted into n-pentane and treated with ethereal hydrogen chloride to give the title compound as a colourless solid, m.p. 143°-144° C. (from methanol/diethyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05773463 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-a53d191abf1c49e3afe739de28ecb880 |
| Source note | uspto-grants-1998_06 |