HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1,2,3,4-Tetrahydro-Beta-Carboline-3-Carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | L-Tryptophan | HCID 6305 | — |
| Product | 1,2,3,4-Tetrahydro-Beta-Carboline-3-Carboxylic Acid | HCID 98285 | — |
Reaction Steps
To a mixture of 0.1 NH2SO4 (150 mL) and 37% formaldehyde (80 mL) was added portionwise L-tryptophane (50 g, 245 mmol) with stirring. After being stirred for 4 h at room temperature, the white solid separated out was collected by filtration. The solid cake was washed with water and dried to give 1,2,3,4-tetrahydro-pyrido[3,4-b]indole-3-carboxylic acid, 41 g, (78%); mp 275-276° C. (lit.18 mp 280-282° C.). 1H NMR (DMSO-d6) δ 2.84 (1H, m, CH2), 3.16 (1H, m, CH2), 3.66 (1H, m, CH2), 4.23 (1H, m, CH2), 4.38 (1H, m, CH), 6.98-7.02 (1H, m, ArH), 7.13-7.16 (1H, m, ArH), 7.32-7.34 (1H, m, ArH), 7.45-7.48 (1H, m, ArH), 11.03 (1H, brs, exchangeable, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703951B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-f31a8e07c06942959be25c6c93660fd9 |
| Source note | uspto-grants-2014_04 |