Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191211Generated: November 3, 2026

Sodium hydride → HCID 86649378, compound

https://huagongshe.com/reaction/2191211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 66599117HCID 66599117—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86649378HCID 86649378121.5%

Reaction Steps

Charge a vial with (S)-benzyl 7,9-dimethyl-5-(2-methyl-2H-tetrazol-5-ylamino)-2,3,4,5-tetrahydro-1H-benzo[b]azepine-1-carboxylate (100 mg 246 μmoles), NaH (23 mg 60% in mineral oil, 575.1 μmoles) and THF (9.2 ml, 24.6 mmoles). (Alternatively, potassium tert-butoxide in DMF can be used in place of NaH and THF.) Stir the reaction mixture at RT for 10 m. Add 3,5 bis(trifluoromethyl)benzylbromide (173.8 mg 566.2 μmoles) dropwise over 30 min. After about 19 h, add NaH (10 mg, 60% mineral oil) and stir for an additional 1 h. Partition the reaction mixture between EtOAc (50 mL) and brine (2×25 mL). Collect the organic layers and dry over Na2SO4. Filter and then concentrate the filtrate to yield an oil. Partition the oil between ACN (50 mL) and heptane (2×25 mL). Collect the CAN layer; dry to yield an oil (189 mg) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329688B2
Source datasetuspto-grants-2012_12
ORD IDord-2c7963344ed94ba9aa75e0769b93c6ec
Source noteuspto-grants-2012_12