HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537447Generated: October 29, 2026
3-Methylbutanal → HCID 68156815, compound
https://huagongshe.com/reaction/537447
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methylbutanal | HCID 11552 | — |
| Reactant | Ethyl 4-iodobenzoate | HCID 142891 | — |
| Reactant | HCID 178461733 | HCID 178461733 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68156815 | HCID 68156815 | 94% |
Reaction Steps
To a solution of ethyl 4-iodobenzoate (20 g, 72 mmol) in tetrahydrofuran (200 mL) at −40° C. was added isopropylmagnesium chloride lithium chloride (62 mL, 80 mmol, 1.3 M in THF) dropwise, maintaining the internal temperature below −30° C. The mixture was stirred for 30 minutes and 3-methylbutanal (8.68 g, 101 mmol) was then added dropwise, maintaining the internal temperature below −35° C. Following the addition, the reaction was allowed to stir for 15 minutes at −35° C. and was then allowed to warm to room temperature. The reaction was quenched with 1 N aqueous hydrochloric acid (400 mL), and the mixture was extracted with ethyl acetate (2×200 mL). The organics were washed with brine (200 mL) and water (200 mL), dried over sodium sulfate, filtered and concentrated to give ethyl 4-(1-hydroxy-3-methylbutyl)benzoate (16 g, 93%) as an oil. 1H NMR (400 MHz, CDCl3, δ): 7.95 (d, J=8.4 Hz, 2H), 7.34 (d, J=8.4 Hz, 2H), 4.73-4.76 (m, 1H), 4.28-4.33 (m, 2H), 1.60-1.71 (m, 2H), 1.41-1.46 (m, 1H), 1.31-1.39 (m, 3H), 0.87-0.92 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859591B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-5c51bd14718f434096b06fd50de1e7de |
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| Source note | uspto-grants-2014_10 |
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