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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970241Generated: October 29, 2026

Iodine → HCID 85962995, compound

https://huagongshe.com/reaction/970241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 85962992HCID 85962992—
SolventTetrahydrofuranHCID 8028—
ProductHCID 85962995HCID 8596299579%

Reaction Steps

Nonadeca-1,8,10-triyne (0.802 g, 3.133 mmol) and anhydrous THF (96 mL) was cooled to −78° C. in a dry flask under nitrogen. LiN[Si(CH3)]2 (LHMDS) in THF (3.76 mmol) was added to the reaction mix slowly via dry syringe. In a separate flask I2(9.55 g, 3.76 mmol) was dissolved in dry THF (20 mL). The iodine solution was added dropwise to the nonadeca-1,8,10-triyne solution until reaction completion (notably becoming orange-red). The reaction was stirred for 30 min, and slowly warmed to room temperature. The reaction was extracted with diethyl ether and 1M K2S2O3. The organic phase was dried over anhydrous MgSO4, and concentrated by evaporation to yield 1-iodo-nonadeca-1,8,10-triyne (0.93 g, 2.45 mmol). GC/MS showed no starting material remaining. 79% yield; 1H NMR (CDCl3) δ 2.15-2.33 (m, 6H, CH2—C≡C), 1.48 (m, 6H, CH2—C—C≡C), 1.33-1.39 (m, 2H, CH2—CH2—CH3), 1.28 (m, 10H, C—CH2—C), 0.85 (t, 3H, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07311943B2
Source datasetuspto-grants-2007_12
ORD IDord-c6c0447949ed4c9a9fe60d2c58356df9
Source noteuspto-grants-2007_12