HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784415Generated: October 25, 2026
Formaldehyde → 6-Ethoxy-1,2,3,4-tetrahydroisoquinoline
https://huagongshe.com/reaction/1784415
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-(3-Ethoxyphenyl)ethan-1-amine | HCID 2758765 | — |
| Product | 6-Ethoxy-1,2,3,4-tetrahydroisoquinoline | HCID 45116 | — |
Reaction Steps
A stirred mixture of 2-(3-ethoxy-phenyl)-ethylamine (7.0 g, 42 mmol) and 37% aqueous formaldehyde solution (3.5 mL) was heated at 110° C. for 30 minutes. The stirring was stopped and the upper water layer was removed by pipette. To the resulting mixture water (5.25 mL) and concentrated HCl (10.5 mL) were added followed by heating 100° C. for 30 minutes. After allowing to cool to room temperature the mixture was evaporated to dryness and recrystallised from acetone yielding the subtitled compound as a cream solid (2.73 g). MH+ 178. 1H NMR δ (DMSO) 1.27-1.35 (3H, t), 2.88-3.03 (2H, t), 3.18-3.40 (2H, br, t), 3.95-4.08 (2H, q), 4.10-4.22 (2H, m), 6.74-6.85 (2H, m), 7.05-7.15 (1H, m), 9.33-9.55 (2H, br.s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504392B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-b0f73e038fb84aee8e0beadb0311b188 |
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| Source note | uspto-grants-2009_03 |
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