HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17945Generated: October 25, 2026
Formaldehyde → 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile
https://huagongshe.com/reaction/17945
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-Hydroxybenzyl cyanide | HCID 26548 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile | HCID 59166221 | 9,757.2% |
Reaction Steps
To a solution of (4-hydroxyphenyl)acetonitrile (17.3 g, 0.13 mol) in toluene (350 mL) were added paraformaldehyde (39.0 g, 0.43 mmol) and toluene-4-sulfonic acid monohydrate (2.5 g, 13 mmol) at room temperature. The reaction mixture was heated at reflux for 1 hour. Toluene was removed by evaporation. Water (150 mL) and ethyl acetate (150 mL) were added. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organics were washed with brine, dried over Na2SO4 and evaporated under vacuum. The residue was separated by preparative HPLC to give 2-(4H-benzo[d][1,3]dioxin-6-yl)acetonitrile (7.35 g, 32%). 1H NMR (400 MHz, CDCl3) δ 7.07-7.11 (m, 1H), 6.95-6.95 (m, 1H), 6.88 (d, J=11.6 Hz, 1H), 5.24 (s, 2H), 4.89 (s, 2H), 3.67 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741321B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-97fdd375e7ac4a87a776ef17a63e595e |
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| Source note | uspto-grants-2010_06 |
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