HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17944Generated: October 30, 2026
Formaldehyde → 2-(4H-benzo[d][1,3]dioxin-7-yl)acetonitrile
https://huagongshe.com/reaction/17944
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2-(3-Hydroxyphenyl)acetonitrile | HCID 13781042 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4H-benzo[d][1,3]dioxin-7-yl)acetonitrile | HCID 59166216 | 47.9% |
Reaction Steps
To a solution of (3-hydroxyphenyl)acetonitrile (75.0 g, 0.56 mol) in toluene (750 mL) was added paraformaldehyde (84.0 g, 2.80 mol) and toluene-4-sulfonic acid monohydrate (10.7 g, 56.0 mmol) at room temperature. The reaction mixture was heated at reflux for 40 minutes. 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 anhydrous Na2SO4 and evaporated under vacuum. The residue was separated by preparative HPLC to give 2-(4H-benzo[d][1,3]dioxin-7-yl)acetonitrile (4.7 g, 5%). 1H NMR (300 MHz, CDCl3) δ 6.85-6.98 (m, 3H), 5.25 (d, J=3.0 Hz, 2H), 4.89 (s, 2H), 3.69 (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-909d7aa9f45b4b6587bf61feb026f72e |
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| Source note | uspto-grants-2010_06 |
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