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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethyl-1-butanolHCID 7358—
ReactantTriphenylphosphineHCID 11776—
Reactantmethyl 7-hydroxy-8-methyl-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69516883—
ReactantN-ethoxycarbonyliminocarbamateHCID 86599450—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69517745HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-f8b1e96440804089968478409072b215
Source noteuspto-grants-2007_08