HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → trans-1-(2-Hydroxymethylanilino)-2-methylaminoindane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | trans-1-(2-Methoxycarbonylanilino)-2-ethoxycarbonylaminoindane | HCID 54064549 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | trans-1-(2-Hydroxymethylanilino)-2-methylaminoindane | HCID 15807945 | 89% |
Reaction Steps
A solution of trans 1-(2-methoxycarbonylanilino)-2-ethoxycarbonylaminoindane (1.73 kg; 4.9 moles) in diethyl ether (36 l) was added dropwise to a suspension of lithium aluminium hydride (900 g; 23.7 moles) in diethyl ether (28 l), under nitrogen, over a period of ca 1.5 h. After stirring overnight at room temperature the excess lithium aluminium hydride was carefully decomposed with water (2.5 l), and 10% sodium hydroxide (30 l) and water (5 l) was added. The organic layer was separated and the aqueous phase extracted with two further portions of ether (2×20 l). The combined extracts were washed (water), dried (MgSO4) and concentrated. Crystallisation from ethyl acetate/pet. ether afforded the title compound (1.17 Kg; 89%) m.p. 113°-4°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04585588 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-4f87077736c6411cafce5b0c07042bc6 |
| Source note | uspto-grants-1986_04 |