HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542799Generated: October 27, 2026
Hydrochloric Acid → HCID 178482122, compound
https://huagongshe.com/reaction/542799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-Methylisatoic anhydride | HCID 25160 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178434708 | HCID 178434708 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178482122 | HCID 178482122 | — |
Reaction Steps
A solution of butyl lithium in hexane (1.6M, 67.5 ml) was added to a stirred mixture of 5-methyltetrazole (4.54 g), and dry tetrahydrofuran (200 ml) at 0°. After stirring for 1 hour, 1-methyl-1H-3,1-benzoxazine-2,4-dione (9.6 g) was added and stirring continued for 65 hours at room temperature. The mixture was poured into water (300 ml) and acidified with 5N hydrochloric acid (12 ml). The organic phase was separated and the aqueous phase was extracted with dichloromethane (2×200 ml). The organic phases were combined, dried over anhydrous magnesium sulphate, and evaporated. The resulting solid was triturated with dichloromethane:industrial methylated spirit 9:1 (200 ml). The solid product was collected and recrystallised from ethyl acetate to give the novel compound 1-(2-methylaminophenyl)-2-(1H-tetrazol-5-yl)ethanone, m.p. 199°-201°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04659718 |
|---|
| Source dataset | uspto-grants-1987_04 |
|---|
| ORD ID | ord-24b858e7989e4c8cb4417b9e72ca772f |
|---|
| Source note | uspto-grants-1987_04 |
|---|