HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883817Generated: October 25, 2026
Stannous Chloride → 4-(Benzyloxy)-3,5-dichloroaniline
https://huagongshe.com/reaction/883817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | 2-(Benzyloxy)-1,3-dichloro-5-nitrobenzene | HCID 59509764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-(Benzyloxy)-3,5-dichloroaniline | HCID 18543171 | — |
Reaction Steps
Tin(II) chloride (22 g, 98 mmol) was added to a stirring solution of 2-(benzyloxy)-1,3-dichloro-5-nitrobenzene (5.8 g, 19 mmol) in ethanol (80 mL), and the resulting suspension was heated to 70° C. After 1 h the mixture was cooled to room temperature and diluted with ethyl acetate (200 mL). The mixture was poured into brine (100 mL) and the resulting emulsion stirred with sodium potassium tartrate solution (200 mL). The mixture was extracted with ethyl acetate and the combined organic layers dried (MgSO4), filtered and concentrated in vacuo to afford 4-(benzyloxy)-3,5-dichloroaniline that was used directly in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08236984B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-3cc40db0e4aa49bfb82c4e603f980a5f |
|---|
| Source note | uspto-grants-2012_08 |
|---|