Home Cart Sign in  
Chemical Structure| 1822-57-7 Chemical Structure| 1822-57-7

Structure of 1822-57-7

Chemical Structure| 1822-57-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1822-57-7 ]

CAS No. :1822-57-7
Formula : C10H9Cl2N
M.W : 214.09
SMILES Code : ClCC1=CC=NC2=CC=CC=C12.[H]Cl
MDL No. :MFCD18157690

Safety of [ 1822-57-7 ]

Application In Synthesis of [ 1822-57-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1822-57-7 ]

[ 1822-57-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6281-32-9 ]
  • [ 1822-57-7 ]
YieldReaction ConditionsOperation in experiment
65% With thionyl chloride; In dichloromethane; at 20℃; for 1h;Inert atmosphere; 4-(Chloromethyl)quinoline hydrochloride MDE 32016 To a solution of <strong>[6281-32-9]quinolin-4-ylmethanol</strong> MDE 32014 (0.28 g, 1.76 mmol) in dry CH2Cl2 (18 mL) at 0 C. under N2 in a 50 mL round-bottomed flask equipped with a magnetic stirrer was added dropwise SOCl2 (2.6 mL, 36.0 mmol) and the mixture was stirred for 1 h at RT. The volatiles were then removed at 40 C. under vacuum and the residue was taken up in CH2Cl2 (20 mL) before concentration back to dryness at 40 C. under vacuum (done 3 times) to give 4-(chloromethyl)quinoline hydrochloride MDE 32016 as an off-white solid (246 mg, 65% yield). MW: 214.09; Yield: 65%; Off-white solid; Mp ( C.): 40.1 1H-NMR (CD3OD, delta): 4.91 (s, 2H, CH2), 8.07 (dd, 1H, J=7.7 Hz, ArH), 8.21-8.35 (m, 3H, 3*ArH), 8.59 (d, 1H, J=8.6 Hz, ArH), 9.26 (d, 1H, J=5.6 Hz, ArH). 13C-NMR (CD3OD, delta): 42.0, 122.3, 122.9, 126.4, 128.3, 131.7, 136.3, 139.1, 146.0, 156.9. MS-ESI m/z (% rel. Int.): 178 ([MH]+, 35Cl, 100), 180 ([MH]+, 37Cl, 32).
48% With thionyl chloride; In dichloromethane; Step b) Preparation of 4-(Chloromethyl)quinoline Hydrochloride 4-Quinolinemethanol (21.5 g, 135 mmol) was treated with thionyl chloride (32.12 g, 270 mmol) in 500 mL of methylene chloride and refluxed for 0.5 hour. The reaction was cooled to 0 C. for 1 hour, filtered and washed with cold methylene chloride and ether to afford, after air-drying, 13.87 g (65 mmol, 48% yield) of the product as a dark tan solid, m.p. 193-195 C. (dec). 1 H NMR (DMSO-d6, 400 MHz) delta: 12.3 (br s, 1H), 9.26 (d, J=5.3 Hz, 1H), 8.47 (d, J=9.5 Hz, 1H), 8.46 (d, J=9.8 Hz, 1H), 8.13 (d, J=5.3 Hz, 1H), 8.11 (ddd, J=8.3, 7.0, 1.3 Hz, 1H), 7.97 (ddd, J=8.0, 7.0, 1.0 Hz, 1H), 5.52 (s, 2H) MS(EI), m/z (rel. intensity)=179 (25), 177 (M+, 67), 159 (37), 142 (100), 130 (77) IR (KBr) v: 3440, 2940, 2900, 2470, 1605, 1545, 1385, 1280, 1220, 840, 750 cm-1 Anal. Calcd. for C10 H8 ClN. HCl: C,56.10; H, 4.24; N, 6.54. Found: C, 56.01; H, 4.10; N, 6.39.
With thionyl chloride; In dichloromethane; at 20℃; for 1h; Thionylchloride (1.45 mL, 20 mmol) was added dropwise to a solution of carbinol (18) (1.5 g, 9.4 mmol) in DCM at room temperature. The reaction mixture was stirred at room temperature for 1 h and evaporated to give (15.13) (2.0 g) as a crude product.
 

Historical Records

Technical Information

Categories