HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72996Generated: October 30, 2026
Lithium borohydride → HCID 58550743, compound
https://huagongshe.com/reaction/72996
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 3-formyl-4-isopropoxybenzoate | HCID 18922523 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58550743 | HCID 58550743 | 100.3% |
Reaction Steps
Methyl 3-formyl-4-isopropoxy-benzoate (180 mg, 0.8 mmol) was dissolved in tetrahydrofuran (5 mL) and lithium borohydride (35 mg, 1.6 mmol) was added. The reaction mixture was stirred at room temperature for 30 minutes, then quenched with methanol (3 mL). The reaction mixture was neutralized by the addition of a saturated aqueous solution of sodium bicarbonate (3 mL) and extracted with ethyl acetate (3×10 mL). The organic layers were washed with brine solution (1×10 mL), dried over sodium sulfate, filtered and concentrated in vacuo to yield methyl 3-(hydroxymethyl)-4-isopropoxy-benzoate (180 mg, 99%) as a viscous liquid. ESI-MS m/z calc. 224.3. Found 225.3 (M+1)+; Retention time: 1.26 minutes (3 min run); 1H NMR (400 MHz, DMSO) δ 8.09 (s, 1H), 7.89 (d, J=8.6 Hz, 1H), 7.13 (d, J=8.6 Hz, 1H), 5.25 (t, J=5.6 Hz, 1H), 4.86-4.68 (m, 1H), 4.54 (d, J=5.6 Hz, 2H), 3.87 (s, 3H), 1.35 (d, J=6.0 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828996B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8672319b962146e289b8e75cdcc3cb7b |
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| Source note | uspto-grants-2014_09 |
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