ChemicalBook > CAS DataBase List > 4-Boc-2-(hydroxymethyl)homomorpholine

4-Boc-2-(hydroxymethyl)homomorpholine

Product Name
4-Boc-2-(hydroxymethyl)homomorpholine
CAS No.
1174020-52-0
Chemical Name
4-Boc-2-(hydroxymethyl)homomorpholine
Synonyms
tert-Butyl 2-(hydroxymethyl);-1,4-oxazepane-4-carboxylate;4-Boc-1,4-oxazepan-2-methanol;4-Boc-2-hydroxymethyl-1,4-oxazepane;4-Boc-2-(hydroxymethyl)homomorpholine;tert-Butyl 2-(hydroxyMethyl)-1,4-oxazepane-4-carboxylate;1,4-Oxazepine-4(5H)-carboxylic acid, tetrahydro-2-(hydroxymethyl)-, 1,1-dimethylethyl ester
CBNumber
CB32534452
Molecular Formula
C11H21NO4
Formula Weight
231.29
MOL File
1174020-52-0.mol
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4-Boc-2-(hydroxymethyl)homomorpholine Property

Boiling point:
337.8±27.0 °C(Predicted)
Density 
1.090±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
14.36±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

AK Scientific
Product number
2839AA
Product name
tert-Butyl2-(hydroxymethyl)-1,4-oxazepane-4-carboxylate
Packaging
250mg
Price
$130
Updated
2021/12/16
Matrix Scientific
Product number
126724
Product name
tert-Butyl2-(hydroxymethyl)-1,4-oxazepane-4-carboxylate
Purity
>95%
Packaging
1g
Price
$316
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
AGR0000199
Product name
4-BOC-2-(HYDROXYMETHYL)HOMOMORPHOLINE
Purity
95.00%
Packaging
1G
Price
$321.3
Updated
2021/12/16
Matrix Scientific
Product number
126724
Product name
tert-Butyl2-(hydroxymethyl)-1,4-oxazepane-4-carboxylate
Purity
>95%
Packaging
5g
Price
$1098
Updated
2021/12/16
Ambeed
Product number
A156935
Product name
tert-Butyl2-(hydroxymethyl)-1,4-oxazepane-4-carboxylate
Purity
98+%
Packaging
250mg
Price
$53
Updated
2021/12/16
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4-Boc-2-(hydroxymethyl)homomorpholine Chemical Properties,Usage,Production

Synthesis

24424-99-5

1207254-23-6

1174020-52-0

Step-4: Synthesis of tert-butyl 2-(hydroxymethyl)-1,4-oxoazepane-4-carboxylate To a dichloromethane solution of (1,4-oxoazepan-2-yl)methanol (550 mg, 4.2 mmol) was added triethylamine (1.2 mL, 8.4 mmol) and di-tert-butyl dicarbonate (1.1 equiv., 1 mL, 4.61 mmol) sequentially at 0°C. The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the reaction was quenched with saturated NaHCO3 solution and then extracted with ethyl acetate. The organic layer was washed sequentially with water and brine, dried over anhydrous Na2SO4 and concentrated to give the target product tert-butyl 2-(hydroxymethyl)-1,4-oxoazepane-4-carboxylate (800 mg, 82.6% yield). 1H NMR (400 MHz, DMSO-d6) δ: 4.68 (m, 1H), 3.95 (m, 1H), 3.70 (m, 1H), 3.54-2.98 (m, 6H), 1.74 (m, 2H), 1.46 (m, 1H), 1.39 (s, 4H).

References

[1] Patent: US2010/168080, 2010, A1. Location in patent: Page/Page column 89
[2] Journal of Medicinal Chemistry, 2017, vol. 60, # 6, p. 2227 - 2244

4-Boc-2-(hydroxymethyl)homomorpholine Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Boc-2-(hydroxymethyl)homomorpholine Suppliers

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1174020-52-0, 4-Boc-2-(hydroxymethyl)homomorpholineRelated Search:


  • 4-Boc-2-(hydroxymethyl)homomorpholine
  • tert-Butyl 2-(hydroxyMethyl)-1,4-oxazepane-4-carboxylate
  • -1,4-oxazepane-4-carboxylate
  • tert-Butyl 2-(hydroxymethyl)
  • 1,4-Oxazepine-4(5H)-carboxylic acid, tetrahydro-2-(hydroxymethyl)-, 1,1-dimethylethyl ester
  • 4-Boc-1,4-oxazepan-2-methanol
  • 4-Boc-2-hydroxymethyl-1,4-oxazepane
  • 1174020-52-0