HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618404Generated: October 30, 2026
Acetonitrile → 3-(3-Bromophenyl)-3-hydroxypropanenitrile
https://huagongshe.com/reaction/1618404
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3-Bromophenyl)-3-hydroxypropanenitrile | HCID 57608363 | — |
Reaction Steps
To a stirred mixture of THF (200 mL) and CH3CN (7.8 mL, 148 mmol) cooled to −50° C., was added KOtBu (18.16 g, 162 mmol) in portions by maintaining the temperature at −50° C. After stirring for 30 min, 3-bromobenzaldehyde (25 g, 135 mmol) was charged maintaining the same internal temperature. After stirring for 30 min, the reaction mixture was warmed to 0° C. and stirred for additional 3 h. This was recooled to −10° C. and quenched with excess water. Extraction with ethyl acetate yielded the crude product, which was purified by flash chromatography (0 to 20% EtOAc-hexanes gradient) to give 23 as light yellow oil. Yield (21 g, 69%): 1H NMR (400 MHz, DMSO-d6) δ 7.61 (s, 1H), 7.49 (bd, J=7.8 Hz, 1H), 7.47 (bd, J=7.6 Hz, 1H), 7.34 (t, J=7.6 Hz, 1H), 6.09 (d, J=4.4 Hz, 1H), 4.92 (m, 1H), 2.81-2.95 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08766007B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-bd179ddeeaa04a228c6ae17de9d763f6 |
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| Source note | uspto-grants-2014_07 |
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