HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256092Generated: October 31, 2026
HCID 4577356, compound → 2-Hydroxycyclopentadecan-1-one
https://huagongshe.com/reaction/256092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 4577356 | HCID 4577356 | — |
| Reactant | HCID 20165421 | HCID 20165421 | — |
| Reactant | 2-Oxocyclopentadecyl acetate | HCID 20165422 | — |
| Reactant | HCID 20165424 | HCID 20165424 | — |
| Product | 2-Hydroxycyclopentadecan-1-one | HCID 543400 | — |
Reaction Steps
Thirty grams each of 2-hydroxycyclopentadecanone, 2-hydroxycyclotridecanone, 2-acetoxycyclopentadecanone, 2-acetoxycyclotridecanone, and 2-hydroxycyclohexadecanone obtained through acyloin condensation was dissolved in 200 ml of an organic solvent shown in Table 1. The resulting solution was placed in a reaction apparatus equipped with a reflux condener having a water trap, a stirrer, and a dropping funnel, and 40 g of a zinc powder was dispersed therein. The mixture was allowed to react under reflux by adding 150 ml of 12N hydrochloric acid dropwise over a period of 1.5 hours. During the reaction, the aqueous layer in the trap was intermittently withdrawn in the case of using toluene, xylene, or cyclohexane as an organic solvent. In the case of using methyl ethyl ketone, the whole amount of the liquid reserved in the trap (about 90 ml) was intermittently withdrawn.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04700007 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-2fa0293147e846818e8c0069ae9cbc78 |
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| Source note | uspto-grants-1987_10 |
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