HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 2-(2-bromo-1-benzothiophen-3-yl)-2-(tert-butoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-(1-benzothiophen-3-yl)-2-(tert-butoxy)acetate | HCID 70813710 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-(2-bromo-1-benzothiophen-3-yl)-2-(tert-butoxy)acetate | HCID 70813729 | 45% |
Reaction Steps
N-bromosuccinimide (67 mg, 0.37 mmol) was added at room temperature to a stirred solution of methyl 2-(1-benzothiophen-3-yl)-2-(tert-butoxy)acetate (4b) (70 mg, 0.25 mmol) in acetonitrile (2 mL) under a nitrogen atmosphere. After 20 hours, water (10 mL) was added and the reaction mixture was extracted with dichloromethane (2×10 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to afford the desired product (4c) as a pale oil (40 mg, 0.11 mmol, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-44f5cbeafb6b4fdc9a1c743a8fb6ef00 |
| Source note | uspto-grants-2016_01 |