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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417939Generated: October 29, 2026

Dibutyltin dichloride → HCID 66648191, compound

https://huagongshe.com/reaction/417939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibutyltin dichlorideHCID 12688—
ReactantPhenylsilaneHCID 12752—
Reactant3-Furancarboxaldehyde, tetrahydro-HCID 157568—
ReactantHCID 24956161HCID 24956161—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66648191HCID 6664819122.6%

Reaction Steps

A mixture of Example 12 (50 mg, 0.15 mmol), tetrahydrofuran-3-carboxaldehyde (30 mg, 0.15 mmol), phenylsilane (0.04 mL, 0.3 mmol) and dibutyltin dichloride (5 mg, 0.015 mmol) in THF (3 mL) was heated to 100° C. under microwave irradiation for 40 min. After cooling to r.t., the mixture was partitioned between EtOAc (50 mL) and water (50 mL). The organics were washed with brine (50 mL), dried (MgSO4) and concentrated in vacuo. The crude material was purified by prep HPLC to give the title compound as a yellow solid (14 mg, 22%). δH (CDCl3) 1.08 (6H, s), 1.56-1.71 (2H, m), 1.98-2.13 (1H; m), 2.35 (2H, s), 2.43-2.57 (1H, m), 2.68 (2H, s), 3.03 (1H, d, J 6.8 Hz), 3.52-3.59 (1H, m), 3.65-3.76 (1H, m), 3.78-3.91 (2H, m), 4.08-4.15 (2H, m), 4.16-4.22 (2H, m), 6.32 (1H, dd, J 8.7, 2.4 Hz), 6.73 (1H, d, J 8.7 Hz), 7.10 (1H, d, J 2.6 Hz). LCMS (ES+) 414 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093238B2
Source datasetuspto-grants-2012_01
ORD IDord-3339ba47d4d34ab5a937fa69840652e0
Source noteuspto-grants-2012_01