HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[6-Benzyloxy-2,2-dimethylchroman-4-yl]-N-ethylmethanesulfonamide → N-[2,2-dimethyl-6-hydroxychroman-4-yl]-N-ethyl-methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[6-Benzyloxy-2,2-dimethylchroman-4-yl]-N-ethylmethanesulfonamide | HCID 21264511 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | N-[2,2-dimethyl-6-hydroxychroman-4-yl]-N-ethyl-methanesulfonamide | HCID 17786837 | — |
Reaction Steps
12 g of N-[6-benzyloxy-2,2-dimethylchroman-4-yl]-N-ethylmethanesulfonamide were dissolved in 250 ml of THF/methanol (1:1) and hydrogenated in a shaking duck using Pd/carbon. After absorption of hydrogen was complete, the catalyst was filtered off with suction, the filtrate was concentrated and the residue was crystallized using diisopropyl ether, 7.7 g, m.p. 169-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06177449B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-2a1be54814304987a3e4c44758b8391f |
| Source note | uspto-grants-2001_01 |