HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582019Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 86759440, compound
https://huagongshe.com/reaction/1582019
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1-Naphthaleneacetic Acid | HCID 6862 | — |
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Product | HCID 86759440 | HCID 86759440 | 76% |
Reaction Steps
A mixture of 1-naphthylacetic acid (5) (2.0 g, 0.011 mol), PTSA (200 mg, 1.1 mmol), and diethylene glycol (6) (8 ml, 72.8 mmol) was stirred at 120° C. under N2. The reaction mixture became homogeneous after 1 h, and the stirring was continued for 15 h. After the reaction was completed (confirmed by TLC), the reaction mixture was poured into 50 ml of icewater mixture. The aqueous reaction mixture was extracted by EtOAc (3×50 ml) and dried over anhydrous MgSO4. The crude product was purified by column chromatography (SiO2, EtOAc/hexanes: 8/2) to yield 2.25 g (76%) of 7 as a colorless oil. 1H NMR (CDCl3, 500 MHz, 20° C.): d 7.83 (d, 1H, J=7.1 Hz ), 7.72-7.64 (m, 2H), 7.40-7.26 (m, 4H), 4.11 (t, 2H, J=4.7Hz), 3.96 (s, 2H), 3.46 (overlapped m, 4H), 3.26 (t, 2H, J=4.4 Hz), 1.90 (s, 1H). 13C NMR (CDCl3, 90 MHz, 20° C.): d 171.7, 134.0, 132.2, 130.6, 128.9, 128.2, 126.5, 126.0, 125.7, 123.9, 72.4, 65.8, 64.2, 61.2, 39.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06733883B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-e4dbcb93201a4ed8b8c2a0a57e15f56c |
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| Source note | uspto-grants-2004_05 |
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