Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514220Generated: October 31, 2026

Phenyl Isothiocyanate → HCID 88851620, compound

https://huagongshe.com/reaction/514220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl IsothiocyanateHCID 7673—
ReactantTriethylamineHCID 8471—
ReactantHCID 68158720HCID 68158720—
SolventTetrahydrofuranHCID 8028—
ProductHCID 88851620HCID 8885162033.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

The amine trifluoroacetate salt from Example 5 (0.064 g, 0.135 mmol) was dissolved in THF (0.5 mL). Et3N (0.037 mL, 0.27 mmol) was added, followed by phenyl isothiocyanate (0.020 mL, 0.15 mmol). The resulting dark yellow solution was heated to 80° C. and stirred for 4 h. The solution was cooled to 25° C., loaded directly onto a silica gel column and purified (gradient elution with 15% to 40% to 80% EtOAc in hexanes) to afford the product (0.0222 g, 33%) as a yellow oil: IR νmax 3380, 3218 (br), 1617, 1598, 1518, 1497, 1448, 1356, 1326, 1264, 1221, 1168, 1111, 1065, 986, 910, 851, 756, 732, 694 cm−1; 1H NMR (300 MHz, CDCl3) δ 8.56 (s, 1H), 8.11 (d, J=8.3 Hz, 2H), 7.90 (br s, 1H), 7.78 (d, J=9.0 Hz, 2H), 7.46-7.32 (m, 5H), 7.31-7.21 (m, 5H), 3.10 (br s, 1H), 2.25 (br s, 1H), 1.51-1.30 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C25H20F3N5OS, 495.134; found, 495.1341.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107410B2
Source datasetuspto-grants-2015_08
ORD IDord-bee07ea8cf5a42eda7c38836120e35f3
Source noteuspto-grants-2015_08