HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 13653084, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13653070 | HCID 13653070 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13653084 | HCID 13653084 | 65% |
Reaction Steps
A mixture of 0.577 g of methyl (3S)-6-fluoro-1,2,3,4-tetrahydro-β-carboline-3-carboxylate hydrochloride, 0.32 g of sodium borohydride, 20 ml of ethanol and 10 ml of water is stirred at room temperature for 21 hours, and then further refluxed for 3 hours. After the reaction, insoluble materials are removed by filtration and washed with hot ethanol. The filtrate and washings are combined and concentrated. Water is added to the residue, and crystalline precipitates are collected by filtration and dried, whereby 286 mg of (3S)-3-hydroxymethyl-6-fluoro-1,2,3,4-tetrahydro-β-carboline are obtained as colorless needles. Yield: 65%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04625032 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-7b3db535d3554275906d83bb3facd803 |
| Source note | uspto-grants-1986_11 |