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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928966Generated: October 27, 2026

2-Chloroaniline → 5-(Benzyloxy)-2-((2-chlorophenyl)amino)-3,4-difluorobenzoic acid

https://huagongshe.com/reaction/928966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroanilineHCID 7240—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-Benzoxy-2,3,4-trifluorobenzoic acidHCID 89704915—
SolventTetrahydrofuranHCID 8028—
Product5-(Benzyloxy)-2-((2-chlorophenyl)amino)-3,4-difluorobenzoic acidHCID 8970490389.1%

Reaction Steps

To a solution of 2-chloroaniline (13.91 ml, 137.00 mmol) and 5-benzyloxy-2,3,4-trifluorobenzoic acid (19.33 g, 68.50 mmol) in THF (120 mL) at −78° C. was added LiHMDS (205.5 mL, 1 M in THF, 205.5 mmol) dropwisely under nitrogen atmosphere. The mixture was slowly warmed to room temperature and stirred at this temperature overnight. The reaction was quenched with water (100 mL) and acidified to pH 2-3 with 10% HCl (aq.). The mixture was extracted with ethyl acetate (100 mL×3). The combined organic extracts were washed with water (100 mL) and brine (100 mL) sequentially, dried over Na2SO4, filtered and concentrated in vacuo to afford the desired product (pale yellow solid, 23.80 g, 89.1% yield). 1H NMR (400 MHz, DMSO-d6): δ 13.80 (s, 1H), 8.66 (s, 1H), 7.64 (m, 1H), 7.34 (m, 7H), 6.92 (m, 1H), 6.78 (m, 1H), 5.26 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290468B2
Source datasetuspto-grants-2016_03
ORD IDord-e5749811485d4b2f8bb989b6bb571a4d
Source noteuspto-grants-2016_03