1-HYDROXYMETHYL-3-CYCLOPENTENE
1-HYDROXYMETHYL-3-CYCLOPENTENE Basic information
- Product Name:
- 1-HYDROXYMETHYL-3-CYCLOPENTENE
- Synonyms:
-
- 1-HYDROXYMETHYL-3-CYCLOPENTENE
- Cyclopent-3-enyl-methanol
- 3-Cyclopenten-1-ylMethanol
- cyclopent-3-en-1-ylMethanol
- 3-Cyclopentene-1-Methanol
- Cyclopent-3-ene-1-methanol
- 1-HYDROXYMETHYL-3-CYCLOPENTENE ISO 9001:2015 REACH
- 3-Cyclopentene-1-methanol (7CI, 8CI, 9CI, ACI)
- CAS:
- 25125-21-7
- MF:
- C6H10O
- MW:
- 98.14
- Product Categories:
-
- pharmacetical
- Mol File:
- 25125-21-7.mol
1-HYDROXYMETHYL-3-CYCLOPENTENE Chemical Properties
- Boiling point:
- 105-108 °C
- Density
- 0.975±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 14.93±0.10(Predicted)
- Appearance
- Colorless to light yellow Liquid
1-HYDROXYMETHYL-3-CYCLOPENTENE Usage And Synthesis
Synthesis
7686-77-3
25125-21-7
General procedure for the synthesis of 1-hydroxymethyl-3-cyclopentene from 3-cyclopentenecarboxylic acid: (a) To an anhydrous tetrahydrofuran (100 ml) suspension of lithium aluminium hydride (0.5083 g, 13.37 mmol, 3 eq.), a solution of 3-cyclopentenecarboxylic acid (0.5000 g, 4.45 mmol) was slowly added dropwise at -78°C for a controlled duration of 1 hours. The reaction mixture was stirred continuously at this temperature for 6 h. The reaction was subsequently quenched with 15 ml of 1 M NaOH solution. After continued stirring for 2 h, the reaction mixture was concentrated, washed with ether and dried with anhydrous magnesium sulfate to give the final clarified liquid product cyclopent-3-enylmethanol (3.79 mmol, molecular weight 98.14 g/mol, 85% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 2.12-2.16 (tttt, 1H), 2.49-2.53 (dd, 2H), 3.57-3.58 (d, 3H, J=5.14 Hz), 5.69 (s, 2H).
References
[1] Tetrahedron, 2003, vol. 59, # 5, p. 671 - 676
[2] Journal of the American Chemical Society, 1982, vol. 104, p. 7105
[3] Journal of the Chemical Society, Perkin Transactions 1, 2000, # 14, p. 2175 - 2178
[4] European Journal of Organic Chemistry, 2004, # 2, p. 289 - 303
[5] Journal of Heterocyclic Chemistry, 1989, vol. 26, # 2, p. 451 - 452
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