HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → O-(2,4,6-trimethylbenzyl)hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-carboethoxy-O-(2,4,6-trimethylbenzyl)hydroxylamine | HCID 21441810 | — |
| Product | O-(2,4,6-trimethylbenzyl)hydroxylamine | HCID 22487017 | 71.4% |
Reaction Steps
200 ml of an aqueous solution of 45 g (0.8 mole) of potassium hydroxide was added to 47.5 g (0.2 mole) of the N-carboethoxy-O-(2,4,6-trimethylbenzyl)hydroxylamine prepared as described in Reference Example 1, and the mixture was heated under refluxing for 5 hours. The reaction mixture was allowed to stand for 12 hours, the precipitated crystals were collected by filtration and washed with water to obtain 23.6 g (70.6% yield) of O-(2,4,6-trimethylbenzyl)hydroxylamine. Recrystallization from diethyl ether-petroleum ether (1:3 by volume) yielded a product having a melting point of 54 - 55° C which was subjected to elementary analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017512 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-f2c98ae19d48410999f87af0f73bf082 |
| Source note | uspto-grants-1977_04 |