関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | 6-(benzyloxymethyl)tetrahydro-2H-pyran-3-ol | HCID 58063706 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 6-((benzyloxy)methyl)dihydro-2H-pyran-3(4H)-one | HCID 58063632 | — |
反応手順
DMSO (1.15 mL, 16.2 mmol) was added to a stirred solution of oxalyl chloride (1 mL, 10.8 mmol) in dichloromethane (60 mL) at −78° C. After 10 minutes, a dichlotomethane solution of 6-(benzyloxymethyl)tetrahydro-2H-pyran-3-ol (14) (1.20 g, 5.40 mmol) was added. Stirring was continued for one hour then triethylamine (3.8 mL, 27 mmol) was added and slowly warmed to 0° C. The reaction was poured into saturated NH4Cl solution and the organic phase was washed with brine and dried (NaSO4). The residue was purified over silica gel using EtOAc and hexanes to give 6-(benzyloxymethyl)dihydro-2H-pyran-3(4H)-one (15).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08569283B2 |
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| 出典データセット | uspto-grants-2013_10 |
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| ORD ID | ord-c1f36ece35b8490a87ba36277688477d |
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| 出典メモ | uspto-grants-2013_10 |
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