HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 8-(Aminomethyl)naphthalene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 8-(aminomethyl)naphthalene-2-carboxylate | HCID 14731550 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(Aminomethyl)naphthalene-2-carboxylic acid | HCID 14756563 | 95% |
Reaction Steps
Part C--To a solution of methyl 8-aminomethyl-2-naphthoate (0.75 g, 0.0035 mol) in dry tetrahydrofuran (50 mL), cooled to 0° C., was added a solution of lithium hydroxide (0.5M, 5.83 mL). All was stirred at ambient temperature over 20 hours. Another aliquot of lithium hydroxide was added and all was stirred for an additional 20 hours. The solid was collected and the filtrate was evaporated to dryness under reduced pressure. The solids were triturated with diethyl ether to give 8-aminomethyl-2-naphthoic acid (0.67 g, 0.0033 mol, 95%) as a white solid. mp=223°-225° C.; 1H NMR (DMSO) d 8.6 (s, 1H), 8.1-7.9 (m, 1H), 7.8-7.7 (m, 4H), 7.55-7.5 (m, 1H), 7,45-7.35 (m, 2H), 4.2 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05635477 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-79ebdd1e04094765b5db59826dd52fe3 |
| Source note | uspto-grants-1997_06 |