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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233618Generated: October 31, 2026

Tert-Butyl hypochlorite → HCID 23356090, compound

https://huagongshe.com/reaction/233618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantHCID 23356027HCID 23356027—
SolventDichloromethaneHCID 6344—
ProductHCID 23356090HCID 2335609046%

Reaction Steps

Under argon and at room temperature, was added dropwise 0.820 g (7.6 mmol) of t-butylhypochlorite to a stirred solution containing 1.973 g (7.4 mmol) of the isochroman from step 5 in 75 ml of anhydrous CH2Cl2. The reaction mixture was stirred for 3 hours and then washed successively with 25 ml portions of saturated aqueous sodium thiosulfate, water and brine. After drying over Na2SO4, the organic layer was evaporated and the residue was flash chromatographed with 2.5% ethyl acetate in toluene as the eluting solvent mixture. The title compound was obtained in 46% yield (1.02 g). (MP: 95.0° C.) 1H NMR (200 MHz, CDCl3) δ: 1.35 (t, 3H, J=7.1 Hz, CH3), 2.93 (broad dd, J=16.8, 10.3 Hz, HCHaCHC=O), 3.16 (broad dd, J=16.9, 3.2 Hz, HCHeCHC=O), 3.78 (s, 3H, OCH3), 3.81 (s, 3H, OCH3), 4.27 (dd, J=10.2, 3.3 Hz, --CH), 4.31 (q, 2H, J=7.1Hz, OCH2), 4.63 (broad d, 1H, J=16.2 Hz, HCHa0), 5.01 (d, 1H, J=16.2 Hz, HCHe0), 6.73 (s, 1H, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593970
Source datasetuspto-grants-1997_01
ORD IDord-d34adf19820441419ed16c20627d183a
Source noteuspto-grants-1997_01