HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480542Generated: October 31, 2026
Stearoyl chloride → HCID 88120683, compound
https://huagongshe.com/reaction/480542
Participants
| Role | Name | HCID | Charge |
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| Reactant | Stearoyl chloride | HCID 8212 | — |
| Reactant | HCID 11679335 | HCID 11679335 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 88120683 | HCID 88120683 | 62.2% |
Reaction Steps
Stearoyl chloride (5.45 g; 18 mmol) dissolved in CHCl3 (60 mL) was added dropwise in 1 h to a solution of N2,N2-bis[2-[bis[2-(1,1-dimethylethoxy)-2-oxoethyl]amino]ethyl]-L-lysine 1,1-dimethylethyl ester (13.5 g; 18 mmol) in CHCl3 (300 mL) at 0° C. After 10 min the reaction mixture was allowed to rise to room temperature and TLC analysis showed the complete conversion of the starting materials. The solution was washed with 5% aq. NaHCO3, the organic phase was separated, dried over Na2SO4 and then evaporated under reduced pressure. The crude product was purified by flash chromatography (n-hexane/EtOAc=6/4 (v/v)) to give the desired product (11.3 g; 11.2 mmol). Yield 62%. HPLC: 95% (area %). the 13C-NMR, MS and IR spectra were consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06652834B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-821265a6ab284c16b5c761cb783c1a7f |
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| Source note | uspto-grants-2003_11 |
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