HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844229Generated: October 31, 2026
Methane, dichloromethoxy- → HCID 16738489, compound
https://huagongshe.com/reaction/1844229
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 19701587 | HCID 19701587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16738489 | HCID 16738489 | 94% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946287B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-4cdf1f0d97ba4d118ee5d657203f977a |
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| Source note | uspto-grants-2015_02 |
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