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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 5-Benzoxy-2,3,4-trifluorobenzoic acid | HCID 89704915 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Benzyloxy)-2-((2-chlorophenyl)amino)-3,4-difluorobenzoic acid | HCID 89704903 | 89.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09290468B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-e5749811485d4b2f8bb989b6bb571a4d |
|---|
| Source note | uspto-grants-2016_03 |
|---|