HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445860Generated: October 29, 2026
Boron tribromide → HCID 52951573, compound
https://huagongshe.com/reaction/445860
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Methyl 5-methoxy-2,3-dihydro-1H-indene-2-carboxylate | HCID 53724337 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 52951573 | HCID 52951573 | — |
Reaction Steps
To a solution of methyl 5-methoxy-2,3-dihydro-1h-indene-2-carboxylate (696) (2.35 g, 11.4 mmol) in anhydrous dichloromethane (40 mL) cooled to −78° C. was added boron tribromide (1.5 eq.). The reaction was allowed to stir at −78° C. for 30 minutes, 0° C. for 2 hours, and at room temperature overnight. The reaction mixture was cooled to 0° C. and quenched slowly with methanol. After stirring for 15 minutes a saturated sodium bicarbonate solution was added slowly to the mixture and allowed to stir at 0° C. for 30 minutes. Ethyl acetate was added and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford methyl 5-hydroxy-2,3-dihydro-1H-indene-2-carboxylate (697).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476308B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-6da10ad337854c7fb87256af472d13ca |
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| Source note | uspto-grants-2013_07 |
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