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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970280Generated: October 29, 2026

Water → 2,6,10-Trimethyl-13-nitrotetradeca-2,6,12-triene

https://huagongshe.com/reaction/970280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl EtherHCID 3283—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 72491401HCID 72491401—
Solventtert-ButanolHCID 6386—
Product2,6,10-Trimethyl-13-nitrotetradeca-2,6,12-trieneHCID 7141525637.4%

Reaction Steps

A solution of 1.30 g of 5 in 25 mL of t-butyl alcohol was added to a solution of 30 mL of t-butyl alcohol containing 0.53 g of potassium t-butoxide. The reaction mixture was stirred at room temperature for 1 h, whereupon it was added to 150 mL of ether and 20 mL of H2O. The organic layer was separated and dried over MgSO4, and the solvent was removed by rotary evaporation to afford 0.40 g of racemic RG-4, predominantly the (E)-isomer. 1H NMR δ (ppm) 7.18 (t, CH═CNO2), 5.2 (t, CH3C(CH3)═CH and CH2C(CH3)═CH), 2.19 (s, C═C(CH3)NO2), 2.0 (m, C═CHCH2CH2C(CH3)═CHCH2), 2.2-2.3 (m, CH2C═CNO2), (CH3C═(CH3), 1.6-1.7 (all s, CH3C(CH3)═CHCH2CH2CCH3), 1.2-1.5 (m, CH2CH(CH3)CH2), 0.95 (d, CH2CH(CH3)CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312191B2
Source datasetuspto-grants-2007_12
ORD IDord-33c23296bf64416caeeb89e8bee5073b
Source noteuspto-grants-2007_12