HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969763Generated: October 31, 2026
Palmitoyl chloride → HCID 136333583, compound
https://huagongshe.com/reaction/969763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Palmitoyl chloride | HCID 8206 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2'-Deoxyguanosine monohydrate | HCID 135445705 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 136333583 | HCID 136333583 | — |
Reaction Steps
To a 250 mL flask was added 2′-deoxyguanosine mono-hydrate (5.0 g, 17.5 mmol), triethylamine (3.13 ml, 22.4 mmol) and N,N-dimethyl-4-aminopyridine (0.046 g, 0.37 mmol). N,N-dimethylformamide (130 mL) was added via cannula with stirring and the flask was purged with argon gas. The slurry was allowed to cool 10 minutes in an ice/NaCl bath and palmitoyl chloride (6.3 mL, 20.6 mmol) was added dropwise. The mixture was allowed to stir while it slowly warmed to 25 degrees C. After 72 h, the mixture was poured with stirring into 400 mL of a 1:1 mixture of water and saturated aqueous sodium bicarbonate solution, which mixture had been warmed to about 60 degrees C. The resulting white solid was isolated by suction filtration, washed with water, and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07307166B1 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-e59b8618592f43a8badd0882574dd280 |
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| Source note | uspto-grants-2007_12 |
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