HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 18784610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzoic acid, 2-amino-3,5-diiodo- | HCID 69116 | — |
| Reactant | 2-(Isothiocyanatomethyl)oxolane | HCID 142108 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18784610 | HCID 18784610 | — |
Reaction Steps
A mixture of 2-amino-3,5-diiodobenzoic acid (1.09 g, 2.57 mmol), tetrahydrofurfuryl isothiocyanate (0.35 g, 2.43 mmol) and triethylamine (0.26 g, 2.57 mmol) in 3.5 mL of ethanol was heated to reflux for about 6 h, and then was allowed to cool to room temperature. The ensuing precipitate was filtered and washed with ethanol (1×20 mL), hexanes (1×mL), and then dried to deliver 0.86 g of the title compound of Step A. 1H NMR (400 MHz, Me2SO-d6): δ 1.64-1.75 (m,1H), 1.75-1.85 (m,1H), 1.86-2.0 (m,2H), 3.57-3.65 (m,1H), 3.70-3.81 (m,1H), 4.26-4.34 (m,1H), 4.36-4.44 (m,1H), 4.52-4.60 (m,1H), 8.19 (d,1H), 8.56 (d,1H), 10.1 (br s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06066638 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-66f6af78b9d347c1a41f763f992213ec |
| Source note | uspto-grants-2000_05 |