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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182417Generated: November 1, 2026

Acetyl chloride → HCID 85826160, compound

https://huagongshe.com/reaction/2182417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesium ChlorideHCID 5360315—
ReactantEthyl 4-(tert-butoxy)-3-oxobutanoateHCID 11790264—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 85826160HCID 85826160—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of dry magnesium chloride (0.471 g) in dichloromethane (6 ml) was treated with 4-tert-butoxy-3-oxo-butyric acid ethyl ester [1.00 g, Reference Example 43]. This mixture was cooled to 0° C., then treated with pyridine (0.80 ml), then stirred for 15 minutes at 0° C. and then treated with acetyl chloride (0.352 ml). After stirring for a further 15 minutes at 0° C. and then for 1 hour at ambient temperature the reaction mixture was treated with saturated aqueous ammonium chloride solution and then extracted twice with ethyl acetate. The combined extracts were dried over magnesium sulfate and then evaporated to yield 2-acetyl-4-tert-butoxy-3-oxo-butyric acid ethyl ester (1.15 g) as a yellow oil which was used without further purification. LC-MS (METHOD B): RT=3.16 minutes; 243 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-ad414ab997454fa29f8a16b9588e3ddd
Source noteuspto-grants-2005_05