HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876204Generated: October 30, 2026
8-Hydroxyoctanoic acid → HCID 68194342, compound
https://huagongshe.com/reaction/876204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Hydroxyoctanoic acid | HCID 69820 | — |
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68194342 | HCID 68194342 | 127.5% |
Reaction Steps
8-hydroxyoctanoic acid (100 mg, 0.59 mmol) was dissolved in 1.5 mL of pyridine. To the solution, 4,4′-dimethoxytrityl chloride (237 mg, 0.7 mmol) was added, and the mixture was stirred overnight. The completion of the reaction was confirmed by TLC. Then, the reaction solution was separated into organic and aqueous phases using methylene chloride and water. The organic phase was dried over sodium sulfate, and the solvent was then concentrated under reduced pressure. The residue was purified with a silica gel column (4 g, methylene chloride) to obtain amorphous 8-(4,4′-dimethoxytrityloxy)octanoic acid (348 mg). The obtained 8-(4,4′-dimethoxytrityloxy)octanoic acid was dissolved in 1 mL of methylene chloride. To the solution, 4-aminophenol (70.9 mg, 0.64 mmol), EDC (101.6 mg, 0.88 mmol), HOBT (79 mg, 0.886 mmol), and triethylamine (92 L) were added, and the mixture was stirred overnight. The completion of the reaction was confirmed by TLC. Then, the reaction solution was purified with a silica gel column (5 g, 30%-+50% ethyl acetate/n-hexane) to obtain the amorphous compound (148 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987226B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-1fba6b51f64646a4a060fe1b991f7075 |
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| Source note | uspto-grants-2015_03 |
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