HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854870Generated: October 26, 2026
2-Ethyl-1-butanol → HCID 69517745, compound
https://huagongshe.com/reaction/854870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethyl-1-butanol | HCID 7358 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | methyl 7-hydroxy-8-methyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate | HCID 69516883 | — |
| Reactant | N-ethoxycarbonyliminocarbamate | HCID 86599450 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69517745 | HCID 69517745 | — |
Reaction Steps
Polymer bound PPh3 was suspended in THF for 15 min. Methyl 7-hydroxy-8-methyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate from Step 1 (1.5 g, 5.21 mmole) and 2-ethyl butanol (0.96 mL, 7.81 mmole) were added to the above slurry and stirred for 15 min. Ethyl azodicarboxylate (1.23 mL, 7.81 mmole) was added to above mixture dropwise and the mixture was stirred at room temperature overnight. LCMS indicated product formation and that there was no starting material present. The polymer was filtered off through celite pad and the pad was washed with ether. The filtrate was concentrated and the product mixture was suspended in hexane. The undissolved solid was removed by filtration and the filtrate was evaporated and dried in vacuo to afford yellow solid, (1.76 g, 98%): LCMS m/z395.15 (M+Na). 1H NMR (CDCl3/400 MHz) 7.68 (s, 1H), 7.00 (d, 1H, J=8.4 Hz), 6.48 (d, 1H, J=8.4 Hz), 5.68 (q, 1H, J=7.2 Hz), 3.89 (m, 2H), 3.82 (s, 3H), 2.09 (s, 3H), 1.72 (m, 1H), 1.53 (m, 4H), 0.95 (m, 6H). This ester was of suitable purity to use without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07259266B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-f8b1e96440804089968478409072b215 |
|---|
| Source note | uspto-grants-2007_08 |
|---|