(3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine

Base Information

• Chemical Name: (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine
• CAS No.: 886847-21-8
• Molecular Formula: C₂₂H₂₆BrNO₄
• Molecular Weight: 448.357
• Mol file: 886847-21-8.mol

Synonyms:(3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine

Chemical Property of (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine

There total 3 articles about (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine 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:

(3aR,5S,6S,6aR)-6-(2-Bromo-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde → (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine (886847-21-8)

Guidance literature:

Multi-step reaction with 2 steps

1: CH₂Cl₂ / 12 h / 20 °C

2: NaBH₄ / CH₂Cl₂; methanol / 3 h / 0 - 20 °C

With sodium tetrahydroborate; In methanol; dichloromethane;

DOI:10.1021/jo052420i

Reference yield:

(3aR,5R,6S,6aR)-6-(2-Bromo-benzyloxy)-5-(2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole → (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine (886847-21-8)

Guidance literature:

Multi-step reaction with 4 steps

1: aq. HOAc / 25 °C

2: aq. NaIO₄ / methanol / 0.75 h / 0 °C

3: CH₂Cl₂ / 12 h / 20 °C

4: NaBH₄ / CH₂Cl₂; methanol / 3 h / 0 - 20 °C

With sodium tetrahydroborate; sodium periodate; acetic acid; In methanol; dichloromethane;

DOI:10.1021/jo052420i

Reference yield:

1-[(3aR,5R,6S,6aR)-6-(2-Bromo-benzyloxy)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl]-ethane-1,2-diol → (3aR,5R,6S,6aR)-benzyl-[6-(2-bromo-benzyloxy)-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-ylmethyl]-amine (886847-21-8)

Guidance literature:

Multi-step reaction with 3 steps

1: aq. NaIO₄ / methanol / 0.75 h / 0 °C

2: CH₂Cl₂ / 12 h / 20 °C

3: NaBH₄ / CH₂Cl₂; methanol / 3 h / 0 - 20 °C

With sodium tetrahydroborate; sodium periodate; In methanol; dichloromethane;

DOI:10.1021/jo052420i

Downstream raw materials:

acetic acid 2-acetoxy-10-benzyl-3,3a,5,10,11,11a-hexahydro-2H-1,4-dioxa-10-aza-benzo[a]cyclopenta[e]cycloocten-3-yl ester

(2R,3R,3aS,11aR)-10-benzyl-2,3-isopropylidenedioxy-3,3a,5,10,11,11a-hexahydro-2H-furo[3,2-c][1,5]benzoxazocine