HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895840Generated: October 31, 2026
1,10-Dibromodecane → HCID 15676281, compound
https://huagongshe.com/reaction/1895840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,10-Dibromodecane | HCID 221483 | — |
| Reactant | HCID 178463197 | HCID 178463197 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15676281 | HCID 15676281 | 106% |
Reaction Steps
A 100 mL round-bottom dry flask was purged with Argon gas. Anhydrous DMF (20 mL) and 1,10-dibromdecane (7.5 g, 25 mmol) were mixed and stirred with a stir bar. Sodium acetylide (7.4 g, 18% wt in xylene) was added slowly. The mixture was stirred at 70° C. overnight. The reaction was quenched with DI water (40 ml). The solution was extracted with CH2Cl2 (3×50 mL), re-extracted with DI water (2×50 mL), dried with sodium sulfate overnight, and filtered. After the removal of the solvent by rotoevaporation, 12-bromo-dodec-1-yne (6.5 g) was obtained. The resultant product was added to triethyl phosphate (10.9 ml, 62.5 mmol) and stirred for 24 h at 150° C. After cooling to room temperature, the excess amount of triethyl phosphate was removed under vacuum. A light yellow liquid was obtained (1 g, 20%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518473B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a08e40a5f53546d9bbcf6e9296941dd0 |
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| Source note | uspto-grants-2013_08 |
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