HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → 1-Methoxycarbonyloxy-2,4-dimethoxynaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxy-2,4-dimethoxynaphthalene | HCID 12563547 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Methoxycarbonyloxy-2,4-dimethoxynaphthalene | HCID 14183043 | — |
Reaction Steps
To a solution of 1.27 g of 1-hydroxy-2,4-dimethoxynaphthalene, prepared as shown in Preparations 7 and 8, in 50 ml of tetrahydrofuran was added 0.694 g of methyl chloroformate followed by 0.743 g of triethylamine. The mixture was stirred at room temperature for 16 hours, filtered, then the solvent removed under reduced pressure. The residue was dissolved in diethyl ether, washed with dilute hydrochloric acid and dried over anhydrous sodium sulfate. The ether was removed under reduced pressure and the residue chromatographed on silica gel, eluting with a 1:1 mixture of methylene chloride and hexane, to give 1-methoxycarbonyloxy-2,4-dimethoxynaphthalene, m.p. 128°-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155132 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-51a4826d03fb4eae92e228d814dc4a1d |
| Source note | uspto-grants-1992_10 |