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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472296Generated: October 30, 2026

HCID 86661534, compound → HCID 58069948, compound

https://huagongshe.com/reaction/1472296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86661534HCID 86661534—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTetrabutylammonium FluorideHCID 2724141—
ProductHCID 58069948HCID 5806994839%

Reaction Steps

The silyl protected diester 8 (0.3 g, 0.44 mmol) was dissolved in 1 M solution of TBAF in THF (6 mL) and the solution was kept at 40° C. for two days. The reaction mixture was diluted with water (60 mL) and extracted with ether (2×50 mL). The combined organic layers were concentrated and the thus obtained crude product was purified by column to isolate the pure product (0.097 g, 39%). 1H NMR (400 MHz, CDCl3) δ 5.64 (dt, J=10.9, 7.4 Hz, 2H), 5.52 (dt, J=11.0, 6.8 Hz, 2H), 4.61 (d, J=6.8 Hz, 4H), 3.57 (s, 1H), 2.30 (t, J=7.5 Hz, 4H), 2.09 (q, J=7.1 Hz, 4H), 1.75-1.53 (m, 4H), 1.53-1.06 (m, 36H), 0.88 (t, J=6.8 Hz, 6H). 13C NMR (101 MHz, CDCl3) δ 173.98, 135.64, 123.57, 77.54, 77.22, 76.91, 72.14, 60.41, 37.69, 34.54, 31.89, 29.70, 29.60, 29.44, 29.29, 29.07, 27.76, 25.80, 25.15, 22.82, 14.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012498B2
Source datasetuspto-grants-2015_04
ORD IDord-4e7649020f77468a8ba724c08b7ac79b
Source noteuspto-grants-2015_04