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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921992Generated: October 25, 2026

Salicylic Acid → HCID 178473643, compound

https://huagongshe.com/reaction/921992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylic AcidHCID 338—
ReactantLactic AcidHCID 612—
ReactantPhosphonium, tetrabutyl-, hydroxide (1:1)HCID 84487—
SolventAcetoneHCID 180—
ProductHCID 178473643HCID 178473643—

Reaction Steps

Lactic acid (0.4504 g, 5 mmol), salicylic acid (0.6909 g, 5 mmol) and tetrabutylphosphonium hydroxide (˜40% sol. in H2O) (3.414 g, 5 mmol) were dissolved in 20 ml of acetone and stirred for 15 min at room temperature. The solvent was evaporated and the remaining viscous liquid was dried at 0.01 mbar with stirring for 24 hrs. The desired compound is isolated as a colourless liquid; 1H-NMR (300 MHz, d6-DMSO) δ(ppm)=7.63 (dd, J1=7.6 Hz, J2=1.9 Hz), 7.11 (m, 1H), 6.58 (m, 3H), 4.03 (q, J=6.9 Hz, 1H), 2.17 (m, 8H), 1.42 (m, 16 H), 1.23 (d, 7.0 Hz, 3H), 0.90 (t, J=7.3 Hz, 12 H). 31P-NMR (121.5 MHz, d6-DMSO) δ(ppm)=35.0. 13C-NMR (75 MHz, d6-DMSO) δ(ppm)=176.3, 171.1, 163.0, 131.2, 129.9, 120.5, 117.8, 115.767.3, 23.4 (d, J=15.8 Hz), 22.6 (d, J=4.3 Hz), 20.5, 17.3 (d, J=47.7 Hz), 13.3 (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278134B2
Source datasetuspto-grants-2016_03
ORD IDord-0260974b33fc4dec97a88a0eb2af9a0b
Source noteuspto-grants-2016_03