HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 66740684 | HCID 66740684 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamate | HCID 66740125 | — |
Reaction Steps
To a stirred and cooled (−10° C.) solution of ethyl 1-benzyl-6-methoxy-2,3-dihydro-1H-inden-2-ylcarbamate (668 mg, 2.053 mmol) in dichloromethane (15 ml) under argon was added dropwise 1M tribromoborane (6.16 ml, 6.16 mmol) and stirred over night while the reaction mixture was allowed to warm up to room temperature. Poured into ice water, diluted with dichloromethane, separated organic layer and the aqueous layer was extracted twice with dichloromethane. The combined organic layers were washed subsequently with water, sodium bicarbonate and brine, dried, filtered and evaporated to obtain ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamate as a brown solid. m=620 mg (97%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227930B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-5d5e9374cd434b1498479010135a4a63 |
| Source note | uspto-grants-2016_01 |