تفاعل #60374

ord-d3093c98a1a6452d8b7c295a5c6a4ca5

معادلة التفاعل

NC1CCCc2cc(CO)ccc21
(5-amino-5,6,7,8-tetrahydro-naphthalen-2-yl)-methanol
CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
(BOC)2O
CC(C)(C)OC(=O)NC1CCCc2cc(CO)ccc21
final product
CC(C)(C)OC(=O)NC1CCCc2cc(CO)ccc21
(6-Hydroxymethyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-carbamic acid tert-butyl Ester

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىReaction mixture
  2. 2
    أخرىwas quenched with sat. NH4Cl
  3. 3
    أخرىthe organic layer was isolated
  4. 4
    غسيلwashed with water, brine
  5. 5
    تجفيفdried over MgSO4
  6. 6
    أخرىevaporated in vacuo

الإجراء التجريبي

To a solution of (5-amino-5,6,7,8-tetrahydro-naphthalen-2-yl)-methanol (2.0 g, 11.28 mmol) in CH2Cl2 (20 mL) was added (BOC)2O (2.7 g, 12.41 mmol). The resulting mixture was stirred at RT under N2 gas for 2 h. Reaction mixture was quenched with sat. NH4Cl, the organic layer was isolated and washed with water, brine, dried over MgSO4 and evaporated in vacuo to give the final product. MS m/z: 278.12 (M+H). Calc'd. for C16H23NO3-277.36.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07425631B2uspto-grants-2008_09