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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010520Generated: November 1, 2026

Diethyl Ether → HCID 20591842, compound

https://huagongshe.com/reaction/1010520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAcetic AnhydrideHCID 7918—
Reactant8-Decen-3-ol, 5,9-dimethyl-2-nitro-HCID 11064229—
CatalystSulfuric AcidHCID 1118—
SolventWaterHCID 962—
ProductHCID 20591842HCID 2059184288%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A flask containing 1.3 g of acetic anhydride was cooled to −10° C. with a salt-ice bath, and 2.34 g of 6 was added with magnetic stirring under an N2 atmosphere. After 10-15 min, 2-5 drops of concentrated H2SO4 were added. The reaction mixture was allowed to stir for an additional 10 min, after which it was treated with 40 mL of ether and 10 mL of H2O. The mixture was extracted three times with 15 mL of saturated aqueous sodium bicarbonate and once with 10 mL of saturated aqueous NaCl. The ether layer was dried over anhydrous MgSO4, and the solvent was removed by rotary evaporation to yield 2.41 g (88%) of a mixture of stereoisomers of the nitro acetate 7. 1H NMR δ (ppm) 5.4 (broad m, CH2CH(OAc)), 5.2 (t, C═CH), 4.65 (m, CH3CHNO2), 2.1 (s, CH3CO2), 2.0 (br m, ═CHCH2), 1.60 and 1.65 (both s, CH3C(CH3)═), 1.5 (d, CH3CHNO2), 1.2-1.5 (m, CH2CH(CH3)CH2), 0.95 (d, CH2CH(CH3)CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977315B2
Source datasetuspto-grants-2011_07
ORD IDord-2289f45b84124621bf0d394a7ff98d03
Source noteuspto-grants-2011_07