HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921992Generated: October 25, 2026
Salicylic Acid → HCID 178473643, compound
https://huagongshe.com/reaction/921992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Salicylic Acid | HCID 338 | — |
| Reactant | Lactic Acid | HCID 612 | — |
| Reactant | Phosphonium, tetrabutyl-, hydroxide (1:1) | HCID 84487 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178473643 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278134B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0260974b33fc4dec97a88a0eb2af9a0b |
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| Source note | uspto-grants-2016_03 |
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