HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225935Generated: November 2, 2026
Sodium Hydroxide → N'-tert-butyl-3-methoxy-2-methylbenzohydrazide
https://huagongshe.com/reaction/2225935
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | Benzoyl chloride, 3-methoxy-2-methyl- | HCID 14719554 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N'-tert-butyl-3-methoxy-2-methylbenzohydrazide | HCID 15376235 | 96% |
Reaction Steps
To a stirred suspension of tert-butylhydrazine hydrochloride (397 g, 3.27 mol) in methylene chloride (2 L) at 0° C., was added sodium hydroxide (50% aqueous, 260 g) diluted with water (400 mL). Following this, 3-methoxy-2-methylbenzoyl chloride (140 g, 0.78 mol) in methylene chloride (1 L) and sodium hydroxide (50% aqueous, 80 g) diluted with water (400 mL) were added concurrently at -20° C. After the addition was complete, the reaction mixture was allowed to warm to room temperature and after additional 30 minutes, the organic layer was washed with water (4×500 mL), dried over magnesium sulfate and stripped to yield N-(3-methoxy-2-methylbenzoyl)-N'-tert-butylhydrazine (177 g, 96% yield). 1H-NMR (CDCl3)δppm 1.19 (s, 9H, t-Bu), 2.29 (s, 3H, CH3), 3.87 (s, 3H, OCH3), 6.90 (d, 1H, C-4 or 6), 6.95 (d, 1H, C-4 or C6) 7.19 (dd, 1H, C-5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05344958 |
|---|
| Source dataset | uspto-grants-1994_09 |
|---|
| ORD ID | ord-a5e3b1c6c5de4115b97f3480782cb401 |
|---|
| Source note | uspto-grants-1994_09 |
|---|