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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844229Generated: October 31, 2026

Methane, dichloromethoxy- → HCID 16738489, compound

https://huagongshe.com/reaction/1844229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 19701587HCID 19701587—
SolventDichloromethaneHCID 6344—
ProductHCID 16738489HCID 1673848994%

Reaction Steps

(iPr)2NEt (6.0 mL, 35.0 mmol) was added dropwise to a stirred and cooled (0° C.) solution of alcohol 3a (4.0 g, 16.3 mmol) in CH2Cl2 (50 mL). After 15 min methoxymethylene chloride (MOMCl) (1.6 mL, 28 mmol) was added dropwise over a period of 5 min, and stirring was continued for 1 h. The cold bath was removed, and stirring was continued for 12 h. The reaction mixture was diluted with water (10 mL) and extracted with CH2Cl2. The combined organic extracts were washed with brine, dried over Na2SO4, and evaporated. The residue was purified by flash chromatography using hexanes-ethyl acetate mixture (5:1) as eluent to give compound 4a (4.4 g, 94%) as a colorless liquid. Rf=0.48 (25% EtOAc-hexanes); IR (neat) 2956, 2889, 1606, 1497, 1246, 1100, 1043 cm−1; 1H NMR (300 MHz, CDCl3) δ 7.64 (d, J=1.8 Hz, 1H), 7.31 (dd, J=8.7, 2.1 Hz, 1H), 7.10 (d, J=8.1 Hz, 1H), 5.70 (s, 1H), 5.21 (s, 2H), 4.02 (m, 4H), 3.46 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 154.2, 132.8, 131.4, 126.7, 115.5, 112.6, 102.5, 94.8, 65.1, 56.2; EIMS (m/z, rel intensity) 290 (M++2, 54), 288 (M+, 58), 259 (23), 257 (23), 209 (56), 73 (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946287B2
Source datasetuspto-grants-2015_02
ORD IDord-4cdf1f0d97ba4d118ee5d657203f977a
Source noteuspto-grants-2015_02