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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671453Generated: November 1, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 86629048, compound

https://huagongshe.com/reaction/1671453

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantHCID 86629046HCID 86629046—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86629048HCID 8662904893.1%

Reaction Steps

Following the general procedure for the oxidative cleavage of (4-methoxy)benzyl ethers of Description 19, (1S)-1-phenylethyl (2R)-4-[(3-chloropropyl)sulfonyloxy]-2-[(4-methoxyphenyl)methoxy]-3,3-dimethylbutanoate (35a) (0.42 g, 0.82 mmol), dissolved in a mixture of dichloromethane (DCM) and water (10:1) (3 mL), was treated with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) (220 mg, 0.98 mmol). After work-up, the crude material was purified by silica gel column chromatography using a mixture of ethyl acetate (EtOAc) and hexane (Hxn) as eluent (EtOAc/Hxn=1:1) to provide 300 mg (93% yield) of the title compound (35b) as a colorless oil. Rf=0.39 (EtOAc/Hex=1:2). 1H NMR (400 MHz, CDCl3): δ=1.02 (s, 3H), 1.19 (s, 3H), 1.64 (d, J=6.4 Hz, 3H), 2.30-2.37 (m, 2H), 3.01 (d, J=5.6 Hz, 1H), 3.30-3.33 (m, 2H), 3.67-3.70 (m, 2H), 4.02-4.04 (m, 2H), 4.20 (d, J=9.2 Hz, 1H), 6.02 (q, J=6.8 Hz, 1H), 7.36-7.38 (m, 5H) ppm. MS (ESI) m/z: 414.09 (M+Na)+. The analytical data was consistant with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994218B2
Source datasetuspto-grants-2011_08
ORD IDord-c1e7ea700b5f4f769c37c3483c2c5b5c
Source noteuspto-grants-2011_08