反应 #4168908
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fcc64163056e46b99a1bc61c36d90bbd暂无可渲染的结构数据
O1C(CO)=CC2=CC=CC=C12产品信息
1-苯并呋喃-2-甲醇(CAS 55038-01-2)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fcc64163056e46b99a1bc61c36d90bbd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3e8e12523f2047c0b4f58411d977338e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0887a6de24ec4798b235c0739e49651f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-06c4a53146c94f2dac37ab85d2a465cf反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7b3eeea683fa49fdad5d7568c7844fcb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d31c816f11554ea08c8d3f5e9089fab5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2a5f3617af2d412ba1e07db08522199a反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 36.40 g (139 mmol) of triphenylphosphine are added, all at once and with vigorous stirring, to a solution, cooled to 0° C., of 10.40 g (70 mmol) of 2-hydroxymethyl-benzo[b]furan and 46 g (139 mol) of CBr4 in 220 ml of ether. After stirring for 4 hours at 20° C., the precipitate formed is suctioned off and washed with Et2O; the filtrate is dried and concentrated, and the residue is then chromatographed on silica, eluting with a mixture of cyclohexane/CH2Cl2 =80/20, to yield the expected compound in the form of an oil. the precipitate formed washed with Et2O the filtrate is dried concentrated the residue is then chromatographed on silica eluting with a mixture of cyclohexane/CH2Cl2 =80/20
来源 ID: ord-67e2db7a2c614a93b5e3c1c2ad9f9517反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fcc64163056e46b99a1bc61c36d90bbd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3e8e12523f2047c0b4f58411d977338e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3e8e12523f2047c0b4f58411d977338e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Thionyl chloride (5.14 mL, 70.46 mmol) was added dropwise to a solution of benzofuran-2-methanol (3.58 g, 23.48 mmol) and pyridine (10 drops) in dichloromethane (60 mL). Stirring was continued at room temperature for 18 hours. The mixture was carefully diluted with water and extracted with methylene chloride. The organic extracts were washed with aqueous sodium bicarbonate, dried (MgSO4) and concentrated to afford crude product which was purified by flash column chromatography (10% ethyl acetate/hexanes) to afford 2.77 g (69%) of pure product as a yellow oil. extracted with methylene chloride The organic extracts were washed with aqueous sodium bicarbonate dried (MgSO4) concentrated to afford crude product which was purified by flash column chromatography (10% ethyl acetate/hexanes)
来源 ID: ord-2611c20359a248e0bb5cf59284a8dcb3PubChem References
以下资料来自该化合物的公开数据库参考记录。
