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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385331Generated: October 28, 2026

Ethyl 2-(3-bromo-4-hydroxy-5-nitrophenyl)-4-methylpentanoate → Ethyl 2-(3-amino-5-bromo-4-hydroxyphenyl)-4-methylpentanoate

https://huagongshe.com/reaction/385331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(3-bromo-4-hydroxy-5-nitrophenyl)-4-methylpentanoateHCID 57995502—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductEthyl 2-(3-amino-5-bromo-4-hydroxyphenyl)-4-methylpentanoateHCID 5799556672.7%

Reaction Steps

To a stirred solution compound ethyl 2-(3-bromo-4-hydroxy-5-nitrophenyl)-4-methylpentanoate (6 g), in dry methanol (100 mL) was added Pd(OH)2 under an atmosphere of nitrogen. The reaction mixture was stirred for 5 h under an atmosphere of hydrogen. The reaction mixture was filtered through Celite™, washed with methanol and concentrated to dryness under reduced pressure. The crude material was purified by column chromatography to yield ethyl 2-(3-amino-5-bromo-4-hydroxyphenyl)-4-methylpentanoate (4 g, 72%). 1HNMR (CDCl3, 200 MHz): 6.80 (s, 1H); 6.62 (s, 1H); 5.35 (bs, 1H); 4.13 (q, 2H); 3.41 (t, 1H); 1.93-1.56 (m, 2H); 1.51 (m, 1H); 1.21 (t, 3H), 0.97 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367863B2
Source datasetuspto-grants-2013_02
ORD IDord-a7b6c39a0b73466abea1d757a084f921
Source noteuspto-grants-2013_02