HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Isohexane ethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Tert-butoxy-2-isopropoxybenzo[d]thiazole-7-carbaldehyde | HCID 86619832 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isohexane ethyl acetate | HCID 21882781 | — |
| Product | 5-(Tert-butoxy)-2-isopropoxy-7-vinylbenzo[d]thiazole | HCID 66744186 | — |
Reaction Steps
Ph3PMe.Br (5.0 g) is dissolved in dry tetrahydrofuran (100 ml) under argon. N-butyl lithium (8.8 ml, of 1.6 M solution) is added at room temperature over 10 minutes and reaction mixture stirred for a further 30 minutes. A solution of 5-tert-Butoxy-2-isopropoxy-benzothiazole-7-carbaldehyde (1.25 g) in dichloromethane (40 ml) is added drop wise to the reaction mixture and the reaction mixture is stirred for 4.5 hours at room temperature. The solvent is removed in vacuo, redissolved in ethyl acetate, washed with water (3×), brine (1×), dried over MgSO4, filtered and the solvent removed in vacuo. The title compound is obtained by flash column chromatography (silica, eluent ethyl acetate/iso-hexane 1:9). MS (ES+) m/e 292 (MH+) LCT55980
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076489B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-ef323dbbe8b84368bbcd41d7baaff068 |
| Source note | uspto-grants-2011_12 |