HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → (2,3-Dichloro-6-nitrophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2,3-Dichloro-6-nitrobenzaldehyde | HCID 11218271 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2,3-Dichloro-6-nitrophenyl)methanol | HCID 11160370 | 91.1% |
Reaction Steps
196MBT36 (100 mg, 0.455 mmol) was dissolved in methanol (2 mL). Sodium borohydride (17 mg, 0.455 mmol) was added and the mixture was stirred for 30 minutes at room temperature. Saturated aqueous ammonium chloride (1 mL) was added and extracted with dichloromethane (2×10 mL). The combined organic phases were dried over Na2SO4, filtered and evaporated to give 2,3-dichloro-6-nitrobenzyl alcohol (196MBT46-A, 92 mg, 91%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585877B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-40beb7fda9d44a468b721181526bd306 |
| Source note | uspto-grants-2009_09 |