HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392842Generated: October 25, 2026
p-Toluenesulfonic acid → Methyl 16-(2-tetrahydropyranyloxy)hexadecanoate
https://huagongshe.com/reaction/2392842
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 16-hydroxyhexadecanoate | HCID 3496888 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 16-(2-tetrahydropyranyloxy)hexadecanoate | HCID 12687990 | — |
Reaction Steps
100.26 g (0.35 mol) of methyl 16-hydroxyhexadecanoate, 0.60 g (3.5 mol) of p-toluenesulfonic acid and 350 ml of dichloromethane were introduced into a 1-l flask equipped with a stirrer and a dropping funnel and 32.39 g (0.385 mol) of dihydropyan was dropped thereto under stirring at 0° C. After the completion of the addition, the mixture was stirred at room temperature for additional 1 hour to thereby complete the reaction. Next, the reaction mixture was neutralized by adding 0.59 g (7 mmol) of NaHCO3 and filtered. After distilling off the solvent, crude methyl 16-(2-tetrahydropyranyloxy)hexadecanoate (III-a) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05801258 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-1fdc17b104f3439b9ca85abd0b80a480 |
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| Source note | uspto-grants-1998_09 |
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