HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-4-benzylnitrobenzene → 2-Chloro-4-benzylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-4-benzylnitrobenzene | HCID 22287159 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-4-benzylaniline | HCID 22287345 | 44.9% |
Reaction Steps
A solution of 2-chloro-4-benzylnitrobenzene (Method 29) (0.60 g) in ethyl acetate was treated with 10% Pd/C (0.06 g) under argon. The mixture was then stirred under a hydrogen atmosphere for 10 hours. The mixture was filtered under argon and extracted with aqueous hydrochloric acid (50% v/v, 50 ml). The aqueous layer was separated, basified with 2M aqueous NaOH and extracted with ethyl acetate to give the title compound as an oil (0.237 g). NMR: 3.6 (s, 2H), 5.1 (brs, 2H), 6.7 (d, 1H), 6.9 (dd, 1H), 7.0(d, 1H), 7.1-7.3 (m, 5H), MS (CI): 218 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498275B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-c2ce37d68ef641f2b6b6b956091f8eab |
| Source note | uspto-grants-2002_12 |