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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044801Generated: October 30, 2026

Nitrogen → HCID 178523768, compound

https://huagongshe.com/reaction/1044801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDimethyl SulfideHCID 1068—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178523780HCID 178523780—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178523768HCID 178523768—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of cis-4-benzyloxycarbonylaminocyclohexanecarboxylic acid (417 mg, 1.50 mmol) in THF (15 mL) was added BH3.Me2S complex (2.0 M in THF, 1.5 mL, 3.00 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 1 h30. More BH3.Me2S complex (2.0 M in THF, 1.0 mL, 2.00 mmol) was added at 0° C. followed by NaBH4 (12 mg, 0.30 mmol). The reaction mixture was warmed to rt and stirred at this temperature until completion of the reaction. MeOH was carefully added to quench the reaction, the volatiles were removed under reduced pressure and the residue co-evaporated with MeOH (2×). Purification by FC (hept-EA, 1:0->3:2) gave pure cis-4-benzyloxycarbonylaminocyclohexane-methanol as a colorless oil. TLC:rf (1:2 hept-EA)=0.45. LC-MS-conditions 01: tR=0.82 min; [M+H]+=264.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-e8355445806a46a3ac33fcf739cb36d2
Source noteuspto-grants-2013_10