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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306514Generated: October 26, 2026

Water → HCID 131723470, compound

https://huagongshe.com/reaction/2306514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(3-Buten-1-yl)methyl[2-(2-methyl-1-propyl)-1,3-dithian-2-yl]phenylsilaneHCID 22967180—
CatalystMercuric ChlorideHCID 24085—
SolventAcetonitrileHCID 6342—
ProductHCID 131723470HCID 131723470—

Reaction Steps

To a solution of 44 (6.19 g, 17.7 mmol) in CH3CN (200 mL) was added water (10 mL) and HgCl2 (24 g, 88 mmol). After stirring overnight at rt, the mixture was concentrated and partitioned between water (100 mL) and hexane (200 mL). The organic layer was isolated and the aqueous layer extracted twice with 50 mL portions of hexane. The combined organic extracts were washed with saturated aqueous NaCl and dried over Na2SO4. Concennation to dryness in vacuo at rt gave quantitatively crude ketone 45 as a yellow oil. This ketone was used in the next reaction without further purification: Rf 0.75 (1/19 EtOAc:hexane); 1H NMR (300 MHz, CDCl3) δ 7.54-7.51 (m, 2H), 7.41-7.35 (m, 3H), 5.91-5.78 (m, 1H), 4.99 (dd, J=17.0, 1.7 Hz, 1H), 4.90 (dd, J=10.0, 1.7 Hz, 1H), 2.44 (d, J=6.7 Hz, 2H), 2.16-2.06 (m, 3H), 1.16-1.07 (m, 2H), 0.78 (pd, J=6.7 Hz, 6H), 0.51 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441212B1
Source datasetuspto-grants-2002_08
ORD IDord-c500b139405244ce899246fccd4c01f4
Source noteuspto-grants-2002_08