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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276512Generated: October 30, 2026

Oxalyl chloride → HCID 20638812, compound

https://huagongshe.com/reaction/1276512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 12633598HCID 12633598—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 20638812HCID 20638812—

Reaction Steps

To a solution of 155 mg (1.02 mmol) of 1(R)-phenyl-2(S)-carboxy cyclohex-5-ene (See U.S. Pat. No. 5,750,549, Example 158, Step B) in 3 mL of CH2Cl2 at 0° C. was added oxalyl chloride (100 uL) followed by DMF (1 drop). The reaction was allowed to warm to room temperature. After stirring 1 hour the reaction was concentrated in vacuo, redissolved in CH2Cl2 and concentrated to a yellow solid which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166037
Source datasetuspto-grants-2000_12
ORD IDord-c6c599b1de474d5ea996d4f4c4155529
Source noteuspto-grants-2000_12