HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580756Generated: October 25, 2026
Adipoyl chloride → Ethylidene bis[16-(5-chlorocarbonylpentanoyloxy)-hexadecanoate]
https://huagongshe.com/reaction/580756
Participants
| Role | Name | HCID | Charge |
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| Reactant | Adipoyl chloride | HCID 61034 | — |
| Reactant | Ethylidene bis(16-hydroxyhexadecanoate) | HCID 21711995 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethylidene bis[16-(5-chlorocarbonylpentanoyloxy)-hexadecanoate] | HCID 86754141 | 103.2% |
Reaction Steps
In a three-necked round bottomed flask equipped with a reflux condenser, a glass gas inlet tube and a pressure equalizing dropping funnel was placed freshly distilled adipoyl chloride (2.60 ml, 17.50 mmol) dissolved in absolute chloroform (15 ml). The temperature was raised to ca. 50° C. and under a gentle stream of nitrogen through the solution, a solution of ethylidene bis(16-hydroxyhexadecanoate) (1.0 g, 1.75 mmol) in absolute chloroform (30 ml) was added dropwise and left at this temperature a further 3 hours after addition. The mixture was then cooled to room temperature and quickly transferred into a 50 ml round bottomed flask equipped for distillation under reduced pressure. Chloroform was first distilled off at normal pressure, then oil-pump vacuum was established and excess adipoyl chloride distilled off at ca. 75° C., 5 mbar pressure, leaving the residual title compound (1.56 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05919434 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-84e4216bd6154ab99c7de21ee1d2cd67 |
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| Source note | uspto-grants-1999_07 |
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