HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376792Generated: October 30, 2026
Hydrochloric Acid → HCID 19359164, compound
https://huagongshe.com/reaction/376792
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | HCID 19044177 | HCID 19044177 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19359164 | HCID 19359164 | 87% |
Reaction Steps
A suspension of 4-chloro-3-aminomethylbenzoic acid.circle-solid.HCl (6.7 g, 30 mmol) and triethylamine (9.3 g, 92 mmol) in 50 ml of H2O, was added to a solution of Boc-ON (9.2 g, 38 mmol) in 50 ml of tetrahydrofuran cooled to 0° C. The reaction mixture was stirred at room temperature overnight, and the volatile compounds were removed by concentration under reduced pressure. The residue was diluted with H2O, washed with ether, acidified to pH 3 with 1N HCl, and extracted with ethyl acetate. The extracts were washed with H2O, brine, dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure. This material was triturated with ether-hexane to provide the title compound (7.4 g, 87%) as a white powder. mp 159° C. (dec);
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-02820cd03e0d4c90a0986262f401e3fe |
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| Source note | uspto-grants-2000_02 |
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