Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 849630-82-6 | HCID 39082924 | — |
| Reactant | lithium borohydride THF | HCID 131718764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59639728 | HCID 59639728 | 36% |
Reaction Steps
To a stirred solution of 5-bromo-7-isopropylindoline-2,3-dione (45.1 g, 0.17 mol) in THF (275 ml) at room temperature under a nitrogen atmosphere, was added, via syringe, 2.0 M solution of LiBH4/THF (215 ml) over 30 min. The reaction mixture was stirred at 90° C. for 1 hr, cooled, quenched with distilled water and 5% HCl, and extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, and concentrated under reduced pressure. The crude product was purified by elution from a silica gel column with hexane/EtOAc (9:1) to give (14.5 g, 36%) of the product. 1H NMR (300 MHz, CDCl3) δ 8.18 (b, NH), 7.62 (d, 1H), 7.21 (t, 1H), 7.16 (d, 1H), 6.51 (dd, 1H), 3.20 (m, 1H), 1.38 (d, 6H); ESI (+) MS m/e=239 (MH+), ESI (−) MS m/e=237 (MH−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446122B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-9c9b891b756146a9a64a294eb58338a3 |
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| Source note | uspto-grants-2008_11 |
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