HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708258Generated: November 2, 2026
p-Toluenesulfonic acid → HCID 18961269, compound
https://huagongshe.com/reaction/1708258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Reactant | HCID 18961263 | HCID 18961263 | — |
| Product | HCID 18961269 | HCID 18961269 | — |
Reaction Steps
A mixture of 5.0 g (18.5 mmol) of 1-octadecanol, 5.0 g (16.8 mmol) of 3-(4-carboxymethoxyphenyl)-5-methylbenzofuran-2-one (Compound (101), Example 1) and 1.0 g (5.3 mmol) of p-toluenesulfonic acid is stirred at 200° C. under a slight vacuum (150 mmHg) for about 1 hour. The reaction mixture is then diluted with 60 ml of ligroin and cooled with ice/water. The precipitated product is filtered. Crystallisation of the residue due from ligroin given 7.5 g (81%) of 5-methyl-3-(4-n-octadecyloxycarbonylmethoxyphenyl)benzofuran-2-one, melting pint 85°-87° C. (Compound (105), Table 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356966 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-76ffaab2129e4731964128aaf5788205 |
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| Source note | uspto-grants-1994_10 |
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