2-(Boc-aMinoMethyl)benzyl Alcohol

Base Information

• Chemical Name: 2-(Boc-aMinoMethyl)benzyl Alcohol
• CAS No.: 1333114-86-5
• Molecular Formula: C13H19NO3
• Molecular Weight: 237.299
• Hs Code.: 2924299090
• Mol file: 1333114-86-5.mol

Synonyms:2-(Boc-aMinoMethyl)benzyl Alcohol;Carbamic acid,N-[[2-(hydroxymethyl)phenyl]methyl]-, 1,1-dimethylethyl ester;tert-Butyl 2-(hydroxymethyl)benzylcarbamate;N-Boc-2-(hydroxymethyl)benzylamine

Chemical Property of 2-(Boc-aMinoMethyl)benzyl Alcohol

Chemical Property:

• Boiling Point: 390.8±30.0 °C(Predicted)
• PKA: 12.14±0.46(Predicted)
• PSA: 62.05000
• Density: 1.106±0.06 g/cm3(Predicted)
• LogP: 2.40800
• Storage Temp.: Sealed in dry,Room Temperature

Purity/Quality:

97% ^*data from raw suppliers

2-(Boc-aminomethyl)benzylalcohol ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-(Boc-aMinoMethyl)benzyl Alcohol

There total 1 articles about 2-(Boc-aMinoMethyl)benzyl Alcohol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 46.0%

di-tert-butyl dicarbonate (24424-99-5) + 2-(hydroxymethyl)benzylamine (4152-92-5) → C13H19NO3 (1333114-86-5)

Guidance literature:

In methanol; dichloromethane; at 20 ℃; for 24h;

Reference yield:

C13H19NO3 (1333114-86-5) → C35H41N3O6S (1333114-89-8)

Guidance literature:

Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 14 h / Reflux

3: pyridine / 16 h / 20 °C

With pyridine; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; dichloromethane;

Reference yield:

C13H19NO3 (1333114-86-5) → C26H25N3O4S (1333114-90-1)

Guidance literature:

Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 14 h / Reflux

3: pyridine / 16 h / 20 °C

4: trifluoroacetic acid / dichloromethane / 4 h / 20 °C

With pyridine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In 1,4-dioxane; dichloromethane;

upstream raw materials:

di-tert-butyl dicarbonate

2-(hydroxymethyl)benzylamine

Downstream raw materials:

C₂₆H₃₆N₂O₄

C₃₅H₄₁N₃O₆S

C₂₆H₂₅N₃O₄S

(R)-4-benzyl-5-(quinolin-8-ylsulfonyl)-1,2,5,6-tetrahydrobenzo[f][1,4]diazocin-3(4H)-one

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