HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37726Generated: October 28, 2026
Boron tribromide → HCID 10715977, compound
https://huagongshe.com/reaction/37726
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | methyl (R)-7-(3-acetyl-6-methoxy-2,4,5-trimethylphenyl)-7-(4-fluorophenyl)heptanoate | HCID 10812460 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10715977 | HCID 10715977 | 82.9% |
Reaction Steps
A solution of methyl (R)-7-(3-acetyl-6-methoxy-2,4,5-trimethylphenyl)-7-(4-fluorophenyl)heptanoate (2.0 g, 4.7 mmol) in dichloromethane (10 ml) was added dropwise to boron tribromide (2.0 ml, 5.3 g, 21.0 mmol) in dichloromethane (30 ml) at -78° C. The temperature of the reaction solution was elevated gradually to room temperature, and the reaction solution was stirred for 6 hours at the same temperature. To the reaction solution was was added ice-water at 0° C., and the mixture was extracted with ethyl acetate. The organic layer was washed with water, a saturated aqueous solution of sodium chloride in the order mentioned, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was subjected to a silica gel column chromatography to give (R)-7-(3-acetyl-6-hydroxy-2,4,5-trimethylphenyl)-7-(4-fluorophenyl)heptanoic acid (1.56 g). Physico-chemical properties and spectral data are shown in [Table 5].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420363 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-ca138925fce14f1aacf12f939a9cf3c1 |
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| Source note | uspto-grants-1995_05 |
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