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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963022Generated: October 30, 2026

Sulfuryl chloride → HCID 10922235, compound

https://huagongshe.com/reaction/1963022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantBenzyl acetoacetateHCID 142266—
SolventChloroformHCID 6212—
ProductHCID 10922235HCID 1092223599.6%

Reaction Steps

To a solution of benzyl 3-oxobutanoate (15 g, 78 mmol) in chloroform (150 mL) at 0° C. was added sulfuryl chloride (6.35 mL, 78 mmol) during a period of 20 min. The ice bath was removed and reaction mixture was allowed to warm to room temperature and stirred for 4 h. The solvent was evaporated and the crude product was diluted with EtOAc (250 mL). The organic layer was washed with H2O (100 mL), separated, dried over MgSO4 and concentrated to give the desired product as a light yellow oil (17.6 g, 99% yield). 1H NMR (CDCl3) δ 2.31 (s, 3H), 4.80 (s, 1H), 5.25 (s, 2H), 7.30-7.42 (m, 5H). LCMS, [M−H]+=225.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415386B2
Source datasetuspto-grants-2013_04
ORD IDord-dcf29df94a1a4a208c28f00117ca2423
Source noteuspto-grants-2013_04