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3-METHYL-3-(TOLUENESULFONYLOXYMETHYL)OXETANE

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3-METHYL-3-(TOLUENESULFONYLOXYMETHYL)OXETANE Basic information

Product Name:
3-METHYL-3-(TOLUENESULFONYLOXYMETHYL)OXETANE
Synonyms:
  • 3-METHYL-3-OXETANEMETHANOL P-TOLUENESULFONATE
  • 3-METHYL-3-(TOLUENESULFONYLOXYMETHYL)OXETANE
  • (3-methyl-3-oxetanyl)methyl 4-methylbenzenesulfonate
  • 3-Methyl-3-(p-toluenesulfonyloxyMethyl)oxetane, 98%
  • (3-Methyloxetan-3-yl)Methyl 4-Methylbenzenesulfonate
  • (3-Methyloxetan-3-yl)
  • (3-Methyloxetan-3-yl)Methyl p-tosylate
  • (3-methyloxetan-3-yl)methyl 4-methylbenzene-1-sulfonate
CAS:
99314-44-0
MF:
C12H16O4S
MW:
256.32
Mol File:
99314-44-0.mol
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3-METHYL-3-(TOLUENESULFONYLOXYMETHYL)OXETANE Chemical Properties

Melting point:
50-51°
Boiling point:
381.1±15.0 °C(Predicted)
Density 
1.218±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
Solid
color 
Off-white
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Safety Information

HazardClass 
IRRITANT
HS Code 
2904100090
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3-METHYL-3-(TOLUENESULFONYLOXYMETHYL)OXETANE Usage And Synthesis

Definition

ChEBI: (3-Methyl-3-oxetanyl)methyl 4-methylbenzenesulfonate is a benzenesulfonate ester.

Synthesis

3143-02-0

98-59-9

99314-44-0

General procedure for the synthesis of (3-methyloxetan-3-yl)methyl 4-methylbenzenesulfonate from 3-methyl-3-hydroxymethoxetane and p-toluenesulfonyl chloride: Step 1: To a solution of (3-methyloxetan-3-yl)methanol (1 g, 9.79 mmol) in dichloromethane (15 ml) was added triethylamine (2.71 ml, 19.58 mmol) followed by p-toluenesulphonyl chloride (1.867 g, 9.79 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 3 to 5 hours. Upon completion of the reaction, the reaction mixture was quenched with water, the organic layer was extracted with ethyl acetate and purified by column chromatography to afford the title compound (3-methyloxetan-3-yl)methyl 4-methylbenzenesulfonate (1.875 g) as a white solid in 74.7% yield. Product characterization data: 1H NMR (DMSO-d6, 300 MHz): δ 7.82 (d, J = 8.1 Hz, 2H), 7.51 (d, J = 8.1 Hz, 2H), 4.25 (d, J = 5.7 Hz, 2H), 4.19 (d, J = 6.0 Hz, 2H), 4.11 (s, 2H), 2.43 (s, 3H), 1.18 (s, 3H); MS (ESI): m/z 279.0 (M + Na).

References

[1] Chemistry of Materials, 2016, vol. 28, # 18, p. 6628 - 6636
[2] Organic Syntheses, 2002, vol. 79, p. 216 - 216
[3] Patent: WO2018/75698, 2018, A1. Location in patent: Paragraph 00272
[4] Journal of Organic Chemistry, 1998, vol. 63, # 11, p. 3631 - 3646
[5] Tetrahedron, 2001, vol. 57, # 8, p. 1497 - 1507

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