HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376809Generated: October 25, 2026
Triethylamine → N-(BOC)-8-aminomethyl-2-naphthoic acid
https://huagongshe.com/reaction/376809
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | 8-(Aminomethyl)naphthalene-2-carboxylic acid | HCID 14756563 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(BOC)-8-aminomethyl-2-naphthoic acid | HCID 14756565 | 61.8% |
Reaction Steps
Part D--A solution of 8-aminomethyl-2-naphthoic acid (0.50 g, 0.03025 mol) and triethylamine (0.038 mL, 0.028 30 g, 0.000275 mol) in aqueous tetrahydrofuran (50%, 5 mL) was added, portionwise as a solid, 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (0.068 g, 0.000275 mol). All was stirred at ambient temperature over 5 hours. The solution was concentrated to half volume and extracted with diethylether. The aqueous layer was then acidified to a pH of 1.0 using hydrochloric acid (1N) and then extraced with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give the title compound, N-(BOC)-8-aminomethyl-2-naphthoic acid (0.050 g, 0.00017 mol) as a white solid. mp=190-191° C.; 1H NMR (DMSO) d 13.1 (bs, 1H), 8.8 (s, 1H), 8.0 (q, 2H, J=7.9 Hz), 7.9 (d, 1H, J=8.1 Hz), 7.6 (t, 1H, J=7.5 Hz), 7.65-7.55 (m, 2H), 4.6 (d, 2H, J=5.5 Hz), 1.4 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06022523 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-ff8ae35276ae456385f10cbf06943b3c |
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| Source note | uspto-grants-2000_02 |
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